FDA Letter API

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 More Warning Letters Warning Letters About Warning and Close-Out Letters 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