Zep Inc.
FDA inspection history in Emerson, Georgia, 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 Emerson, Georgia.
Cited most
Across all Zep observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.165(e)Testing and release for distribution1
- 21 CFR 211.166(b)Stability testing1
- 21 CFR 211.170(b)Reserve samples1
The complete Zep file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Emerson, Georgia
One Form 483 · 2024 · 12 observations
Latest: Form 483, Oct 24, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-24 | 483 Form 483 | Emerson, Georgia | 12 | $99 |
Investigators on these documents
FEI number 3003906462 · most recent document Oct 24, 2024
About Zep Inc.
How many FDA Form 483s has Zep Inc. received?
FDA Intel has 1 Form 483 on file for Zep Inc.; the most recent is dated Oct 24, 2024.
When was Zep Inc. last inspected by FDA?
The most recent FDA inspection document on file for Zep Inc. is a Form 483 dated Oct 24, 2024, for the site in Emerson, Georgia.
What did FDA cite at Zep Inc.?
The regulations cited most in the observations on file for Zep Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.165(e) (Testing and release for distribution), 1 time.