Unilever Manufacturing (US), Inc.
FDA inspection history in Jonesboro, Arkansas, 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 Jonesboro, Arkansas.
Cited most
Across all Unilever Manufacturing (US) observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Unilever Manufacturing (US) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Jonesboro, Arkansas
One Form 483 · 2020 · 2 observations
Latest: Form 483, Mar 10, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-03-10 | 483 Form 483 | Jonesboro, Arkansas | 2 | $99 |
Investigators on these documents
FEI number 3006642851 · most recent document Mar 10, 2020
About Unilever Manufacturing (US), Inc.
How many FDA Form 483s has Unilever Manufacturing (US), Inc. received?
FDA Intel has 1 Form 483 on file for Unilever Manufacturing (US), Inc.; the most recent is dated Mar 10, 2020.
When was Unilever Manufacturing (US), Inc. last inspected by FDA?
The most recent FDA inspection document on file for Unilever Manufacturing (US), Inc. is a Form 483 dated Mar 10, 2020, for the site in Jonesboro, Arkansas.
What did FDA cite at Unilever Manufacturing (US), Inc.?
The regulations cited most in the observations on file for Unilever Manufacturing (US), Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.