Thornton Industries, Inc
FDA inspection history in Morris, Illinois, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Morris, Illinois.
Cited most
Across all Thornton Industries observations on file
- 21 CFR 211.110(a)(3)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122(d)Materials examination and usage criteria1
- 21 CFR 211.165(c)Testing and release for distribution1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Thornton Industries file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Morris, Illinois
One Form 483 · 2020 · 4 observations
Latest: Form 483, Mar 4, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-03-04 | 483 Form 483 | Morris, Illinois | 4 | $99 |
Investigators on these documents
FEI number 3002837627 · most recent document Mar 4, 2020
About Thornton Industries, Inc
How many FDA Form 483s has Thornton Industries, Inc received?
FDA Intel has 1 Form 483 on file for Thornton Industries, Inc; the most recent is dated Mar 4, 2020.
When was Thornton Industries, Inc last inspected by FDA?
The most recent FDA inspection document on file for Thornton Industries, Inc is a Form 483 dated Mar 4, 2020, for the site in Morris, Illinois.
What did FDA cite at Thornton Industries, Inc?
The regulations cited most in the observations on file for Thornton Industries, Inc are 21 CFR 211.110(a)(3) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time; 21 CFR 211.165(c) (Testing and release for distribution), 1 time.