Teva API India Ltd- Malanpur
FDA inspection history in Malanpur, 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 Malanpur, India.
Cited most
Across all Teva API India Ltd- Malanpur observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.160General requirements1
The complete Teva API India Ltd- Malanpur file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Malanpur, India
One Form 483 · 2019 · 4 observations
Latest: Form 483, Apr 16, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-16 | 483 Form 483 | Malanpur, India | 4 | $99 |
FEI number 3008256596 · most recent document Apr 16, 2019
About Teva API India Ltd- Malanpur
How many FDA Form 483s has Teva API India Ltd- Malanpur received?
FDA Intel has 1 Form 483 on file for Teva API India Ltd- Malanpur; the most recent is dated Apr 16, 2019.
When was Teva API India Ltd- Malanpur last inspected by FDA?
The most recent FDA inspection document on file for Teva API India Ltd- Malanpur is a Form 483 dated Apr 16, 2019, for the site in Malanpur, India.
What did FDA cite at Teva API India Ltd- Malanpur?
The regulations cited most in the observations on file for Teva API India Ltd- Malanpur are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.160 (General requirements), 1 time.