Alchymars ICM SM Private Limited
Letter data
- Company
- Alchymars ICM SM Private Limited
- Recipient
- Mr. K. Nagaradjan | General Manager and Director | Alchymars ICM SM Private Limited | A-14 & 20 SIDCO Pharmaceutical Complex | Alathur, Chengalpattu District | 603110 | Tamil Nadu | India
- Issue date
- 2023-01-31
- Posted date
- Not available
- FDA office
- Center for Drug Evaluation and Research | CDER
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 542879
- Reference number
- Not available
- FEI
- 3005216842
- 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
Alchymars ICM SM Private Limited
MARCS-CMS 542879 —
January 31, 2023
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Reference #:
FEI 3005216842
Product:
Drugs
Recipient:
Recipient Name
Mr. K. Nagaradjan
Recipient Title
General Manager and Director
Alchymars ICM SM Private Limited
A-14 & 20 SIDCO Pharmaceutical Complex
Alathur, Chengalpattu District
603110
Tamil Nadu
India
Issuing Office:
Center for Drug Evaluation and Research | CDER
United States
Dear Mr. Nagaradjan:
The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-18-35 dated February 16, 2018.
Based on our evaluation, it appears that you have addressed the deviations 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 deviations be observed during a subsequent inspection or through other means.
Sincerely,
/S/
Marisa Heayn
Compliance Officer
Division of Drug Quality II
Content current as of:
02/03/2023
Regulated Product(s)
Drugs