Chromo Laboratories India Private Limited
FDA inspection history in Sangareddy, India, 2020 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2020: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Sangareddy, India.
- 2024One Form 483, at Sangareddy, India.
- 2024The longest 483 on file: 9 observations over 9 pages at Sangareddy, India.
Cited most
Across all Chromo Laboratories India Private Limited observations on file
- 21 CFR 211.192Production record review4
- 21 CFR 211.67Equipment cleaning and maintenance4
- 21 CFR 211.160General requirements2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.25Personnel qualifications2
The complete Chromo Laboratories India Private 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
Sangareddy, India
Two Form 483s · 2020 to 2024 · 18 observations
Latest: Form 483, Aug 10, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-08-10 | 483 Form 483 | Sangareddy, India | 9 | $99 |
| 2020-01-24 | 483 Form 483 | Sangareddy, India | 9 | $99 |
Investigators on these documents
FEI number 3008771562 · most recent document Aug 10, 2024
About Chromo Laboratories India Private Limited
How many FDA Form 483s has Chromo Laboratories India Private Limited received?
FDA Intel has 2 Form 483s on file for Chromo Laboratories India Private Limited; the most recent is dated Aug 10, 2024.
When was Chromo Laboratories India Private Limited last inspected by FDA?
The most recent FDA inspection document on file for Chromo Laboratories India Private Limited is a Form 483 dated Aug 10, 2024, for the site in Sangareddy, India.
What did FDA cite at Chromo Laboratories India Private Limited?
The regulations cited most in the observations on file for Chromo Laboratories India Private Limited are 21 CFR 211.192 (Production record review), 4 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 4 times; 21 CFR 211.160 (General requirements), 2 times.