LUPIN LIMITED
FDA inspection history in Ankleshwar, India, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Ankleshwar, India.
Cited most
Across all LUPIN LIMITED observations on file
- 21 CFR 211.188Batch production and control records1
The complete LUPIN LIMITED file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ankleshwar, India
One Form 483 · 2022 · 1 observation
Latest: Form 483, Aug 19, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-19 | 483 Form 483 | Ankleshwar, India | 1 | $99 |
Investigators on these documents
FEI number 3002807510 · most recent document Aug 19, 2022
About LUPIN LIMITED
How many FDA Form 483s has LUPIN LIMITED received?
FDA Intel has 1 Form 483 on file for LUPIN LIMITED; the most recent is dated Aug 19, 2022.
When was LUPIN LIMITED last inspected by FDA?
The most recent FDA inspection document on file for LUPIN LIMITED is a Form 483 dated Aug 19, 2022, for the site in Ankleshwar, India.
What did FDA cite at LUPIN LIMITED?
The regulations cited most in the observations on file for LUPIN LIMITED are 21 CFR 211.188 (Batch production and control records), 1 time.