TAPI Puerto Rico Inc
FDA inspection history in Guayama, Puerto Rico, 2014
- 1
- Form 483
Every document, by year
- Form 483
2014: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One Form 483, at Guayama, Puerto Rico.
Cited most
Across all TAPI Puerto Rico observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete TAPI Puerto Rico file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Guayama, Puerto Rico
One Form 483 · 2014 · 3 observations
Latest: Form 483, Oct 24, 2014 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2014-10-24 | 483 Form 483 | Guayama, Puerto Rico | 3 | $99 |
Investigators on these documents
FEI number 3001104764 · most recent document Oct 24, 2014
About TAPI Puerto Rico Inc
How many FDA Form 483s has TAPI Puerto Rico Inc received?
FDA Intel has 1 Form 483 on file for TAPI Puerto Rico Inc; the most recent is dated Oct 24, 2014.
When was TAPI Puerto Rico Inc last inspected by FDA?
The most recent FDA inspection document on file for TAPI Puerto Rico Inc is a Form 483 dated Oct 24, 2014, for the site in Guayama, Puerto Rico.
What did FDA cite at TAPI Puerto Rico Inc?
The regulations cited most in the observations on file for TAPI Puerto Rico Inc are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.