Professional Compounding Centers of America dba PCCA
Letter data
- Company
- Professional Compounding Centers of America dba PCCA
- Recipient
- Mr. Fabian V. Zaccardo | Chief Operating Officer | Professional Compounding Centers of America dba PCCA | 9901 S. Wilcrest Dr. | Houston | , | TX | 77099-5132 | United States
- Issue date
- 2023-11-21
- Posted date
- Not available
- FDA office
- Center for Drug Evaluation and Research | CDER
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 597638
- 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
Professional Compounding Centers of America dba PCCA
MARCS-CMS 597638 —
November 21, 2023
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About Warning and Close-Out Letters
Product:
Drugs
Recipient:
Recipient Name
Mr. Fabian V. Zaccardo
Recipient Title
Chief Operating Officer
Professional Compounding Centers of America dba PCCA
9901 S. Wilcrest Dr.
Houston
,
TX
77099-5132
United States
Issuing Office:
Center for Drug Evaluation and Research | CDER
United States
Dear Mr. Zaccardo:
The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-21-15 dated January 27, 2021.
Based on our evaluation, it appears that you have addressed the violations 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 FDA 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/
Carla Norris
Compliance Officer
Division of Drug Quality II
Content current as of:
12/01/2023
Regulated Product(s)
Drugs