Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana
FDA inspection history in Aurangabad, India, 2019 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Aurangabad, India.
- 2019The longest 483 on file: 2 observations over 2 pages at Aurangabad, India.
- 2024One Form 483, at Aurangabad, India.
Cited most
Across all Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana 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
Aurangabad, India
Two Form 483s · 2019 to 2024 · 3 observations
Latest: Form 483, Mar 15, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-03-15 | 483 Form 483 | Aurangabad, India | 1 | $99 |
| 2019-05-15 | 483 Form 483 | Aurangabad, India | 2 | $99 |
Investigators on these documents
FEI number 3004995645 · most recent document Mar 15, 2024
About Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana
How many FDA Form 483s has Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana received?
FDA Intel has 2 Form 483s on file for Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana; the most recent is dated Mar 15, 2024.
When was Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana last inspected by FDA?
The most recent FDA inspection document on file for Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana is a Form 483 dated Mar 15, 2024, for the site in Aurangabad, India.
What did FDA cite at Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana?
The regulations cited most in the observations on file for Lupin Ltd. 28-1, Midc Industrial Area, Chikalthana are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.