Rusan Pharma Ltd.
FDA inspection history in Ankleshwar, India, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Ankleshwar, India.
Cited most
Across all Rusan Pharma observations on file
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.160General requirements1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Rusan Pharma file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ankleshwar, India
One Form 483 · 2024
Latest: Form 483, May 3, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-05-03 | 483 Form 483 | Ankleshwar, India | — | $99 |
Investigators on these documents
FEI number 3012065723 · most recent document May 3, 2024
About Rusan Pharma Ltd.
How many FDA Form 483s has Rusan Pharma Ltd. received?
FDA Intel has 1 Form 483 on file for Rusan Pharma Ltd.; the most recent is dated May 3, 2024.
When was Rusan Pharma Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Rusan Pharma Ltd. is a Form 483 dated May 3, 2024, for the site in Ankleshwar, India.
What did FDA cite at Rusan Pharma Ltd.?
The regulations cited most in the observations on file for Rusan Pharma Ltd. are 21 CFR 211.111 (Time limitations on production), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.186 (Master production and control records), 1 time.