DR REDDY'S Laboratories LIMITED
FDA inspection history in Srikakulam, India, 2022 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Srikakulam, India.
- 2025One Form 483, at Srikakulam, India.
- 2025The longest 483 on file: 7 observations over 7 pages at Srikakulam, India.
Cited most
Across all DR REDDY'S Laboratories LIMITED observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
The complete DR REDDY'S Laboratories 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
Srikakulam, India
Two Form 483s · 2022 to 2025 · 9 observations
Latest: Form 483, Jul 18, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-18 | 483 Form 483 | Srikakulam, India | 7 | $99 |
| 2022-07-07 | 483 Form 483 | Srikakulam, India | 2 | $99 |
Investigators on these documents
Jigar R. Patel (1)Patty P. Kaewussdangkul (1)Taichun Qin (1)
FEI number 3012414462 · most recent document Jul 18, 2025
About DR REDDY'S Laboratories LIMITED
How many FDA Form 483s has DR REDDY'S Laboratories LIMITED received?
FDA Intel has 2 Form 483s on file for DR REDDY'S Laboratories LIMITED; the most recent is dated Jul 18, 2025.
When was DR REDDY'S Laboratories LIMITED last inspected by FDA?
The most recent FDA inspection document on file for DR REDDY'S Laboratories LIMITED is a Form 483 dated Jul 18, 2025, for the site in Srikakulam, India.
What did FDA cite at DR REDDY'S Laboratories LIMITED?
The regulations cited most in the observations on file for DR REDDY'S Laboratories LIMITED are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time.