Supriya Lifescience Limited
FDA inspection history in Ratnagiri, 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 Ratnagiri, India.
Cited most
Across all Supriya Lifescience Limited observations on file
- 21 CFR 211.100Written procedures; deviations3
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.166Stability testing1
- 21 CFR 211.188Batch production and control records1
The complete Supriya Lifescience Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ratnagiri, India
One Form 483 · 2019 · 7 observations
Latest: Form 483, Oct 3, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-10-03 | 483 Form 483 | Ratnagiri, India | 7 | $99 |
Investigators on these documents
FEI number 3007497376 · most recent document Oct 3, 2019
About Supriya Lifescience Limited
How many FDA Form 483s has Supriya Lifescience Limited received?
FDA Intel has 1 Form 483 on file for Supriya Lifescience Limited; the most recent is dated Oct 3, 2019.
When was Supriya Lifescience Limited last inspected by FDA?
The most recent FDA inspection document on file for Supriya Lifescience Limited is a Form 483 dated Oct 3, 2019, for the site in Ratnagiri, India.
What did FDA cite at Supriya Lifescience Limited?
The regulations cited most in the observations on file for Supriya Lifescience Limited are 21 CFR 211.100 (Written procedures; deviations), 3 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times.