AARTI PHARMALABS LIMITED
FDA inspection history in Thane, 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 Thane, India.
Cited most
Across all AARTI PHARMALABS LIMITED observations on file
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.194Laboratory records1
The complete AARTI PHARMALABS LIMITED file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Thane, India
One Form 483 · 2022 · 2 observations
Latest: Form 483, Jun 23, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-06-23 | 483 Form 483 | Thane, India | 2 | $99 |
Investigators on these documents
FEI number 3007005296 · most recent document Jun 23, 2022
About AARTI PHARMALABS LIMITED
How many FDA Form 483s has AARTI PHARMALABS LIMITED received?
FDA Intel has 1 Form 483 on file for AARTI PHARMALABS LIMITED; the most recent is dated Jun 23, 2022.
When was AARTI PHARMALABS LIMITED last inspected by FDA?
The most recent FDA inspection document on file for AARTI PHARMALABS LIMITED is a Form 483 dated Jun 23, 2022, for the site in Thane, India.
What did FDA cite at AARTI PHARMALABS LIMITED?
The regulations cited most in the observations on file for AARTI PHARMALABS LIMITED are 21 CFR 211.142 (Warehousing procedures), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.