Nosch Labs Pvt. Ltd.
FDA inspection history in Hyderabad, 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 Hyderabad, India.
Cited most
Across all Nosch Labs Pvt. observations on file
- 21 CFR 211.160General requirements3
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.204Returned drug products1
The complete Nosch Labs Pvt. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Hyderabad, India
One Form 483 · 2024 · 6 observations
Latest: Form 483, Sep 13, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-09-13 | 483 Form 483 | Hyderabad, India | 6 | $99 |
Investigators on these documents
FEI number 3009250999 · most recent document Sep 13, 2024
About Nosch Labs Pvt. Ltd.
How many FDA Form 483s has Nosch Labs Pvt. Ltd. received?
FDA Intel has 1 Form 483 on file for Nosch Labs Pvt. Ltd.; the most recent is dated Sep 13, 2024.
When was Nosch Labs Pvt. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Nosch Labs Pvt. Ltd. is a Form 483 dated Sep 13, 2024, for the site in Hyderabad, India.
What did FDA cite at Nosch Labs Pvt. Ltd.?
The regulations cited most in the observations on file for Nosch Labs Pvt. Ltd. are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time.