Laurus Labs Limited
FDA inspection history in Anakapalli, India, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Anakapalli, India.
Cited most
Across all Laurus Labs Limited observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Laurus Labs Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Anakapalli, India
One Form 483 · 2025 · 1 observation
Latest: Form 483, Jan 31, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-31 | 483 Form 483 | Anakapalli, India | 1 | $99 |
Investigators on these documents
FEI number 3014255847 · most recent document Jan 31, 2025
About Laurus Labs Limited
How many FDA Form 483s has Laurus Labs Limited received?
FDA Intel has 1 Form 483 on file for Laurus Labs Limited; the most recent is dated Jan 31, 2025.
When was Laurus Labs Limited last inspected by FDA?
The most recent FDA inspection document on file for Laurus Labs Limited is a Form 483 dated Jan 31, 2025, for the site in Anakapalli, India.
What did FDA cite at Laurus Labs Limited?
The regulations cited most in the observations on file for Laurus Labs Limited are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.