Centrix, Inc
FDA inspection history in Shelton, Connecticut, 2017 to 2022
- 2
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Shelton, Connecticut.
- 2017The longest 483 on file: 8 observations over 5 pages at Shelton, Connecticut.
- 2022One Form 483, at Shelton, Connecticut.
Cited most
Across all Centrix observations on file
- 21 CFR 211.100(b)Written procedures; deviations3
- 21 CFR 211.125(a)Labeling issuance2
- 21 CFR 211.166(a)Stability testing2
- 21 CFR 211.67(b)Equipment cleaning and maintenance2
- 21 CFR 211.82(a)Receipt and storage of untested components, drug product containers, and closures2
The complete Centrix file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Shelton, Connecticut
Two Form 483s · 2017 to 2022 · 14 observations
Latest: Form 483, Mar 2, 2022 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-02 | 483 Form 483 | Shelton, Connecticut | 6 | $99 |
| 2017-01-31 | 483 Form 483 | Shelton, Connecticut | 8 | $99 |
Investigators on these documents
FEI number 1281412 · most recent document Mar 2, 2022
About Centrix, Inc
How many FDA Form 483s has Centrix, Inc received?
FDA Intel has 2 Form 483s on file for Centrix, Inc; the most recent is dated Mar 2, 2022.
When was Centrix, Inc last inspected by FDA?
The most recent FDA inspection document on file for Centrix, Inc is a Form 483 dated Mar 2, 2022, 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 211.100(b) (Written procedures; deviations), 3 times; 21 CFR 211.125(a) (Labeling issuance), 2 times; 21 CFR 211.166(a) (Stability testing), 2 times.