Alivus Life Sciences Limited
FDA inspection history in Ankleshwar, India, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Ankleshwar, India.
Cited most
Across all Alivus Life Sciences Limited observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.25Personnel qualifications1
The complete Alivus Life Sciences Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ankleshwar, India
One Form 483 · 2019 · 4 observations
Latest: Form 483, Jul 5, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-05 | 483 Form 483 | Ankleshwar, India | 4 | $99 |
Investigators on these documents
FEI number 3004006229 · most recent document Jul 5, 2019
About Alivus Life Sciences Limited
How many FDA Form 483s has Alivus Life Sciences Limited received?
FDA Intel has 1 Form 483 on file for Alivus Life Sciences Limited; the most recent is dated Jul 5, 2019.
When was Alivus Life Sciences Limited last inspected by FDA?
The most recent FDA inspection document on file for Alivus Life Sciences Limited is a Form 483 dated Jul 5, 2019, for the site in Ankleshwar, India.
What did FDA cite at Alivus Life Sciences Limited?
The regulations cited most in the observations on file for Alivus Life Sciences Limited are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.