FDA Letter API

A.D. Berries @ More LLC

Letter data

Company
A.D. Berries @ More LLC
Recipient
Arturo J. Garcia | Owner | A.D. Berries @ More LLC | 1300 N 10th St Ste 330a | McAllen | , | TX | 78501-4392 | United States
Issue date
2025-06-23
Posted date
2025-07-15
FDA office
Division of Southwest Imports
Subject
Foreign Supplier Verification Program (FSVP)
Product
Food & Beverages
CMS ID
710809
Reference number
Not available
FEI
Not available
Inspection dates
2022-11-28 to 2022-11-30

Normalized citations

21 CFR: 21-CFR-1.502(a)21-CFR-112.321-CFR-PART-121-CFR-PART-112

21 U.S.C.: 21-USC-331(zz)21-USC-35021-USC-381(a)(3)21-USC-384

Related FDA links

No related FDA letter link is present in the source index.

Full source text

WARNING LETTER A.D. Berries @ More LLC MARCS-CMS 710809 — June 23, 2025 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Express Delivery Product: Food & Beverages Recipient: Recipient Name Arturo J. Garcia Recipient Title Owner A.D. Berries @ More LLC 1300 N 10th St Ste 330a McAllen , TX 78501-4392 United States Issuing Office: Division of Southwest Imports United States 6/23/2025 WARNING LETTER Re: CMS # 710809 Dear Mr. Garcia: On 5/22/2025 through 5/28/2025, the Food and Drug Administration (FDA) conducted a Foreign Supplier Verification Program (FSVP) inspection of A.D. BERRIES @ MORE LLC located at 1300 N. 10th St Ste 330a, McAllen, TX 78501. We also conducted an inspection on 11/28/2022 through 11/30/2022. These inspections were conducted to determine compliance with the requirements of section 805 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 384a) and the implementing FSVP regulation in 21 CFR part 1, subpart L. The FSVP regulation requires that importers perform certain risk-based activities to verify that human and/or animal food they import into the United States has been produced in a manner that meets applicable U.S. food safety standards. You may find information relating to the FSVP regulation and your responsibilities to comply with the regulation through links in FDA’s FSVP web page at https://www.fda.gov/food/food-safety-modernization-act-fsma/fsma-final-rule-foreign-supplier- verification-programs-fsvp-importers-food-humans-and-animals. During the most recent inspection, we found that you are not in compliance with the requirements of 21 CFR part 1, subpart L for the foods you import. Because of these significant violations, you are not in compliance with section 805 of the FD&C Act. At the conclusion of the inspection, our investigator provided you with a Form FDA 483a FSVP Observations. We acknowledge receipt of your response, dated 6/4/2025 in which you stated that your firm regrets not having been ready with all the documents requested and will be taking the necessary measures to get your files ready for the next inspection. We are unable to evaluate the adequacy of your response because you have not provided any supporting documentation demonstrating your corrective actions. To date, no additional FSVP documents have been received by FD Your significant violations of the FSVP regulation are as follows: You did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR 1.502(a). Specifically, you did not develop an FSVP for any of the foods you import from the foreign suppliers indicated in the attached list, including each of the following foods: Fresh Hass Avocados, imported from (b)(4) , located in (b)(4) Fresh Celery, imported from (b)(4) , located in (b)(4) Fresh Hass Avocados, imported from (b)(4) , located in (b)(4) You import fresh produce that may be considered “covered produce” as defined in 21 CFR 112.3. If after review of the fresh produce that you import you determine that you are an importer of covered produce, you must have an FSVP that demonstrates that your supplier is producing the food in compliance with processes and procedures that provide at least the same level of public health protection as those required under section 419 of the FD&C Act (21 U.S.C. 350h) (regarding standards for produce safety) and the implementing regulations in the Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption (21 CFR part 112). The above violations are not intended to be an all-inclusive list of violations of the FSVP requirements. It is your responsibility to ensure that you are in compliance with section 805 of the FD&C Act and the implementing regulation in 21 CFR part 1, subpart L. This letter notifies you of our concerns and provides you an opportunity to address them. If you do not adequately address this matter, we may take further action. For instance, we may take action under section 801(a)(3) of the FD&C Act (21 U.S.C. 381(a)(3)) to refuse admission of the food you import for which you appear to be in violation of section 805. We may place the food[s] from the identified foreign supplier[s] on detention without physical examination (DWPE) when you import the foods. You can find DWPE information relating to FSVP in Import Alert # 99-41 at http://www.accessdata.fda.gov/cms_ia/ialist.html. In addition, the importation or offering for importation into the United States of an article of food without the importer having an FSVP that meets the requirements of section 805 of the FD&C Act or the FSVP regulation is prohibited under section 301(zz) of the FD&C Act (21 U.S.C. 331(zz)). You should respond in writing within fifteen (15) working days from your receipt of this letter. Your response should address the specific things you are doing to correct any violations. You should include in your response documentation and information that would assist us in evaluating your corrections (e.g., documentation of changes you made, such as a copy of your FSVP, records to demonstrate implementation of your FSVP), and any additional information that you wish to supply relevant to your compliance with the FSVP regulation. If you believe that you are not in violation of the FD&C Act, include your reasoning and any supporting information for our consideration. If you cannot complete all corrections within 15 working days, you should explain the reason for your delay and state when you will correct any remaining violations. Please send your reply to Food and Drug Administration, Attention: Ernesto Barba, Compliance Officer, Division of Southwest Imports, 9725 Via de la Amistad, Ste 200, San Diego, CA 92154. If you have any questions regarding this letter, you may contact Compliance Officer Ernesto Barba via email at Ernesto.Barba@fda.hhs.gov. Please reference CMS # 710809 on any documents or records you provide to us and/ or within the subject line of any email correspondence you send to us. Sincerely, /S/ Todd W. Cato Program Division Director Division of Southwest Imports One Main Place 1201 Main Street, Suite 7200 Dallas, TX 75202 Content current as of: 07/15/2025 Regulated Product(s) Food & Beverages