Gialive SA de CV
Letter data
- Company
- Gialive SA de CV
- Recipient
- Edgar Arroyo Gonzalez | General Director and Legal Representative | Gialive SA de CV | Gialive SA de CV | Carretera a Zacatecas km # 8 | Col. TALAMANTES PONCE | 20311 | Aguascalientes | , | Ags. | Mexico
- Issue date
- 2018-11-27
- Posted date
- Not available
- FDA office
- United States
- Subject
- Not available
- Product
- Not available
- CMS ID
- 470118
- Reference number
- Not available
- FEI
- Not available
- Inspection dates
- Not available
Normalized citations
21 CFR: None found
21 U.S.C.: None found
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
Gialive SA de CV
MARCS-CMS 470118 —
November 27, 2018
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Reference #:
Re:470118
Recipient:
Recipient Name
Edgar Arroyo Gonzalez
Recipient Title
General Director and Legal Representative
Gialive SA de CV
Gialive SA de CV
Carretera a Zacatecas km # 8
Col. TALAMANTES PONCE
20311
Aguascalientes
,
Ags.
Mexico
Issuing Office:
United States
Dear Mr. Edgar Arroyo Gonzalez:
The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter 470118, dated August 28, 2015. Based on our evaluation, it appears that you have addressed the violation(s) contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.
Sincerely,
/S/
Carrie A. Lawlor
Branch Chief
Center for Food Safety and Applied Nutrition
Office of Compliance/ Division of Enforcement/Dietary
Supplement and Labeling Assessment Branch
Content current as of:
11/30/2018