KEKULE PHARMA LIMITED
FDA inspection history in Sangareddy District, India, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Sangareddy District, India.
Cited most
Across all KEKULE PHARMA LIMITED observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete KEKULE PHARMA LIMITED file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Sangareddy District, India
One Form 483 · 2024 · 1 observation
Latest: Form 483, Mar 15, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-03-15 | 483 Form 483 | Sangareddy District, India | 1 | $99 |
Investigators on these documents
FEI number 3009261338 · most recent document Mar 15, 2024
About KEKULE PHARMA LIMITED
How many FDA Form 483s has KEKULE PHARMA LIMITED received?
FDA Intel has 1 Form 483 on file for KEKULE PHARMA LIMITED; the most recent is dated Mar 15, 2024.
When was KEKULE PHARMA LIMITED last inspected by FDA?
The most recent FDA inspection document on file for KEKULE PHARMA LIMITED is a Form 483 dated Mar 15, 2024, for the site in Sangareddy District, India.
What did FDA cite at KEKULE PHARMA LIMITED?
The regulations cited most in the observations on file for KEKULE PHARMA LIMITED are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.