Inga Pharmaceuticals
FDA inspection history in Chennai, India, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Chennai, India.
Cited most
Across all Inga Pharmaceuticals observations on file
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.125Labeling issuance1
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Inga Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chennai, India
One Form 483 · 2017 · 5 observations
Latest: Form 483, Jun 16, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-06-16 | 483 Form 483 | Chennai, India | 5 | $99 |
Investigators on these documents
FEI number 3008327597 · most recent document Jun 16, 2017
About Inga Pharmaceuticals
How many FDA Form 483s has Inga Pharmaceuticals received?
FDA Intel has 1 Form 483 on file for Inga Pharmaceuticals; the most recent is dated Jun 16, 2017.
When was Inga Pharmaceuticals last inspected by FDA?
The most recent FDA inspection document on file for Inga Pharmaceuticals is a Form 483 dated Jun 16, 2017, for the site in Chennai, India.
What did FDA cite at Inga Pharmaceuticals?
The regulations cited most in the observations on file for Inga Pharmaceuticals are 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.125 (Labeling issuance), 1 time.