Lupin Limited
FDA inspection history in Nagpur, India, 2020 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2020: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Nagpur, India.
- 2020The longest 483 on file: 2 observations over 6 pages at Nagpur, India.
- 2023One Form 483, at Nagpur, India.
Cited most
Across all Lupin Limited observations on file
- 21 CFR 211.194(a)(1)Laboratory records2
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete Lupin Limited file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Nagpur, India
Two Form 483s · 2020 to 2023 · 4 observations
Latest: Form 483, Jul 11, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-07-11 | 483 Form 483 | Nagpur, India | 2 | $99 |
| 2020-01-10 | 483 Form 483 | Nagpur, India | 2 | $99 |
Investigators on these documents
Marcellinus D. Dordunoo (1)Raquel Gonzalez Rivera (1)Saundrea A. Munroe (1)
FEI number 3009843207 · most recent document Jul 11, 2023
About Lupin Limited
How many FDA Form 483s has Lupin Limited received?
FDA Intel has 2 Form 483s on file for Lupin Limited; the most recent is dated Jul 11, 2023.
When was Lupin Limited last inspected by FDA?
The most recent FDA inspection document on file for Lupin Limited is a Form 483 dated Jul 11, 2023, for the site in Nagpur, India.
What did FDA cite at Lupin Limited?
The regulations cited most in the observations on file for Lupin Limited are 21 CFR 211.194(a)(1) (Laboratory records), 2 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.