Ajanta Pharma Ltd.
FDA inspection history in Paithan, India, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Paithan, India.
Cited most
Across all Ajanta Pharma observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Ajanta Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Paithan, India
One Form 483 · 2019 · 3 observations
Latest: Form 483, Jun 28, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-06-28 | 483 Form 483 | Paithan, India | 3 | $99 |
Investigators on these documents
FEI number 3006785788 · most recent document Jun 28, 2019
About Ajanta Pharma Ltd.
How many FDA Form 483s has Ajanta Pharma Ltd. received?
FDA Intel has 1 Form 483 on file for Ajanta Pharma Ltd.; the most recent is dated Jun 28, 2019.
When was Ajanta Pharma Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Ajanta Pharma Ltd. is a Form 483 dated Jun 28, 2019, for the site in Paithan, India.
What did FDA cite at Ajanta Pharma Ltd.?
The regulations cited most in the observations on file for Ajanta Pharma Ltd. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.194 (Laboratory records), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.