CEB Michigan Inc
FDA inspection history in Edwardsburg, Michigan, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Edwardsburg, Michigan.
Cited most
Across all CEB Michigan observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
- 21 CFR 211.84(d)(1)Testing and approval or rejection of components, drug product containers, and closures1
The complete CEB Michigan file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Edwardsburg, Michigan
One Form 483 · 2024 · 4 observations
Latest: Form 483, Oct 17, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-17 | 483 Form 483 | Edwardsburg, Michigan | 4 | $99 |
Investigators on these documents
FEI number 3011901066 · most recent document Oct 17, 2024
About CEB Michigan Inc
How many FDA Form 483s has CEB Michigan Inc received?
FDA Intel has 1 Form 483 on file for CEB Michigan Inc; the most recent is dated Oct 17, 2024.
When was CEB Michigan Inc last inspected by FDA?
The most recent FDA inspection document on file for CEB Michigan Inc is a Form 483 dated Oct 17, 2024, for the site in Edwardsburg, Michigan.
What did FDA cite at CEB Michigan Inc?
The regulations cited most in the observations on file for CEB Michigan Inc are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time.