Centrix, Inc.
FDA inspection history in Shelton, Connecticut, 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 Shelton, Connecticut.
Cited most
Across all Centrix observations on file
- 21 CFR 211.166Stability testing1
- 21 CFR 211.82Receipt and storage of untested components, drug product containers, and closures1
The complete Centrix file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Shelton, Connecticut
One Form 483 · 2017 · 2 observations
Latest: Form 483, Jan 31, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-01-31 | 483 Form 483 | Shelton, Connecticut | 2 | $99 |
Investigators on these documents
FEI number 1261412 · most recent document Jan 31, 2017
About Centrix, Inc.
How many FDA Form 483s has Centrix, Inc. received?
FDA Intel has 1 Form 483 on file for Centrix, Inc.; the most recent is dated Jan 31, 2017.
When was Centrix, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Centrix, Inc. is a Form 483 dated Jan 31, 2017, for the site in Shelton, Connecticut.
What did FDA cite at Centrix, Inc.?
The regulations cited most in the observations on file for Centrix, Inc. are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.82 (Receipt and storage of untested components, drug product containers, and closures), 1 time.