Mankind Pharma Limited
FDA inspection history in Kotputli-Behror, India, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Kotputli-Behror, India.
Cited most
Across all Mankind Pharma Limited observations on file
- 21 CFR 211.142Warehousing procedures2
- 21 CFR 211.160General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
The complete Mankind Pharma Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kotputli-Behror, India
One Form 483 · 2025 · 10 observations
Latest: Form 483, Apr 26, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-26 | 483 Form 483 | Kotputli-Behror, India | 10 | $99 |
FEI number 3014150265 · most recent document Apr 26, 2025
About Mankind Pharma Limited
How many FDA Form 483s has Mankind Pharma Limited received?
FDA Intel has 1 Form 483 on file for Mankind Pharma Limited; the most recent is dated Apr 26, 2025.
When was Mankind Pharma Limited last inspected by FDA?
The most recent FDA inspection document on file for Mankind Pharma Limited is a Form 483 dated Apr 26, 2025, for the site in Kotputli-Behror, India.
What did FDA cite at Mankind Pharma Limited?
The regulations cited most in the observations on file for Mankind Pharma Limited are 21 CFR 211.142 (Warehousing procedures), 2 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.