FDA Inspection
Whisk Products IncWhisk Products Inc – FDA Inspection, Feb 18, 2011
Record Details
This FDA Inspection record concerns Whisk Products Inc, with an inspection on February 18, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Whisk Products Inc
- Inspection Date
- February 18, 2011
- Product Type
- Drugs
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ID · c5e629f7-7b74-4e9b-9b05-007ece385cc1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 716530
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
8- 21 CFR 211.101(d)Verification of component addition
- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.194(a)(8)Second person sign off
- 21 CFR 211.165(a)Testing and release for distribution
- 21 CFR 211.180(e)(2)Items to cover on annual reviews
- 21 CFR 211.100(a)Approval and review of procedures
- 21 CFR 211.198(b)(2)Written record of complaint to include findings, follow-up
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Other FDA inspections of Whisk Products Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 26, 2026 | Not classified | Kansas City District Office | Drug Quality Assurance |
| October 22, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 26, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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