FDA Letter API

Prescription Dispensing Laboratories Inc.

Letter data

Company
Prescription Dispensing Laboratories Inc.
Recipient
Raymond L. Solano | President | Prescription Dispensing Laboratories Inc. | 101 Commercial Parkway | Cedar Park | , | TX | 78613 | United States | Rsolano@pdlabs.net
Issue date
2022-02-18
Posted date
Not available
FDA office
Division of Pharmaceutical Quality Operations II
Subject
Not available
Product
Drugs
CMS ID
579286
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 Prescription Dispensing Laboratories Inc. MARCS-CMS 579286 — February 18, 2022 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA Electronic Mail Product: Drugs Recipient: Recipient Name Raymond L. Solano Recipient Title President Prescription Dispensing Laboratories Inc. 101 Commercial Parkway Cedar Park , TX 78613 United States Rsolano@pdlabs.net Issuing Office: Division of Pharmaceutical Quality Operations II United States Mr. Solano: The U.S. Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our warning letter [Case # 579286; Dated: July 30, 2019]. Based on our evaluation, it appears that you have adequately addressed the violations contained in this warning letter. You are expected to take all necessary steps to ensure compliance with the Federal Food, Drug, and Cosmetic Act and FDA’s implementing regulations. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. If you have questions regarding the contents of this letter, you may contact John Diehl via phone at 214-253-5288 or email at john.diehl@fda.hhs.gov. Sincerely, /S/ John W. Diehl, M.S Director, Compliance Branch Office of Pharmaceutical Quality Operations, Division II Content current as of: 02/25/2022 Regulated Product(s) Drugs