Galbraith Laboratories Inc
FDA inspection history in Knoxville, Tennessee, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Knoxville, Tennessee.
Cited most
Across all Galbraith Laboratories observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit1
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment1
The complete Galbraith Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Knoxville, Tennessee
One Form 483 · 2022 · 3 observations
Latest: Form 483, Mar 2, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-02 | 483 Form 483 | Knoxville, Tennessee | 3 | $99 |
Investigators on these documents
FEI number 1000112629 · most recent document Mar 2, 2022
About Galbraith Laboratories Inc
How many FDA Form 483s has Galbraith Laboratories Inc received?
FDA Intel has 1 Form 483 on file for Galbraith Laboratories Inc; the most recent is dated Mar 2, 2022.
When was Galbraith Laboratories Inc last inspected by FDA?
The most recent FDA inspection document on file for Galbraith Laboratories Inc is a Form 483 dated Mar 2, 2022, for the site in Knoxville, Tennessee.
What did FDA cite at Galbraith Laboratories Inc?
The regulations cited most in the observations on file for Galbraith Laboratories Inc are 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time; 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 1 time.