FDA Inspection 1009921 — Whisk Products Inc
The FDA completed an inspection of Whisk Products Inc on April 26, 2017 in Wentzville, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 26, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Wentzville, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1550 | 21 CFR 211.125(f) | Procedures Written and Followed |
| 2406 | 21 CFR 211.194(a)(8) | Identification of Person Performing Review of Lab Records |
| 2619 | 21 CFR 211.198(b)(2) | Complaint Investigation/Follow-Up Findings |