IPR Pharmaceuticals, Inc.
FDA inspection history in Canovanas, Puerto Rico, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Canovanas, Puerto Rico.
Cited most
Across all IPR Pharmaceuticals observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
The complete IPR Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Canovanas, Puerto Rico
One Form 483 · 2018 · 1 observation
Latest: Form 483, Jun 14, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-06-14 | 483 Form 483 | Canovanas, Puerto Rico | 1 | $99 |
Investigators on these documents
FEI number 3003009422 · most recent document Jun 14, 2018
About IPR Pharmaceuticals, Inc.
How many FDA Form 483s has IPR Pharmaceuticals, Inc. received?
FDA Intel has 1 Form 483 on file for IPR Pharmaceuticals, Inc.; the most recent is dated Jun 14, 2018.
When was IPR Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for IPR Pharmaceuticals, Inc. is a Form 483 dated Jun 14, 2018, for the site in Canovanas, Puerto Rico.
What did FDA cite at IPR Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for IPR Pharmaceuticals, Inc. are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time.