Radix Laboratories Incorporated
FDA inspection history in Eau Claire, Wisconsin, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Eau Claire, Wisconsin.
Cited most
Across all Radix Laboratories Incorporated observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Radix Laboratories Incorporated file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Eau Claire, Wisconsin
One Form 483 · 2019 · 3 observations
Latest: Form 483, Jul 25, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-07-25 | 483 Form 483 | Eau Claire, Wisconsin | 3 | $99 |
Investigators on these documents
FEI number 2129004 · most recent document Jul 25, 2019
About Radix Laboratories Incorporated
How many FDA Form 483s has Radix Laboratories Incorporated received?
FDA Intel has 1 Form 483 on file for Radix Laboratories Incorporated; the most recent is dated Jul 25, 2019.
When was Radix Laboratories Incorporated last inspected by FDA?
The most recent FDA inspection document on file for Radix Laboratories Incorporated is a Form 483 dated Jul 25, 2019, for the site in Eau Claire, Wisconsin.
What did FDA cite at Radix Laboratories Incorporated?
The regulations cited most in the observations on file for Radix Laboratories Incorporated are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.