Whisk Products, Inc.
FDA inspection history in Wentzville, Missouri, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Wentzville, Missouri.
Cited most
Across all Whisk Products observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.165(b)Testing and release for distribution1
- 21 CFR 211.166(a)(2)Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Whisk Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Wentzville, Missouri
One Form 483 · 2021 · 7 observations
Latest: Form 483, Oct 22, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-10-22 | 483 Form 483 | Wentzville, Missouri | 7 | $99 |
Investigators on these documents
FEI number 1000056584 · most recent document Oct 22, 2021
About Whisk Products, Inc.
How many FDA Form 483s has Whisk Products, Inc. received?
FDA Intel has 1 Form 483 on file for Whisk Products, Inc.; the most recent is dated Oct 22, 2021.
When was Whisk Products, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Whisk Products, Inc. is a Form 483 dated Oct 22, 2021, for the site in Wentzville, Missouri.
What did FDA cite at Whisk Products, Inc.?
The regulations cited most in the observations on file for Whisk Products, Inc. are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.165(b) (Testing and release for distribution), 1 time; 21 CFR 211.166(a)(2) (Stability testing), 1 time.