Torrent Pharma Inc
Letter data
- Company
- Torrent Pharma Inc
- Recipient
- Mr. Sanjay Gupta | President and CEO | Torrent Pharma Inc | 2091 Hartel Ave. | Levittown | , | PA | 19057 | United States | sanjayqupta@torrentpharma.us
- Issue date
- 2022-03-11
- Posted date
- Not available
- FDA office
- Division of Pharmaceutical Quality Operations I
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 584701
- 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
Torrent Pharma Inc
MARCS-CMS 584701 —
March 11, 2022
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Delivery Method:
Return Receipt Requested
Product:
Drugs
Recipient:
Recipient Name
Mr. Sanjay Gupta
Recipient Title
President and CEO
Torrent Pharma Inc
2091 Hartel Ave.
Levittown
,
PA
19057
United States
sanjayqupta@torrentpharma.us
Issuing Office:
Division of Pharmaceutical Quality Operations I
United States
Dear Mr. Gupta:
The Food and Drug Administration has completed evaluation of Torrent Pharma, Inc. corrective actions in response to our Warning Letter [WL #584701, dated October 28, 2019]. 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/
Craig Swanson
Acting Program Division Director/District Director
Office of Pharmaceutical Quality Operations
Division I
Content current as of:
03/18/2022
Regulated Product(s)
Drugs