FDA Inspection
Whisk Products IncWhisk Products Inc – FDA Inspection, Apr 26, 2017
Record Details
This FDA Inspection record concerns Whisk Products Inc, with an inspection on April 26, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · a1ddd76d-eafd-48f1-b2b1-1e7988d41f4e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1009921
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 211.198(b)(2)Complaint Investigation/Follow-Up Findings
- 21 CFR 211.194(a)(8)Identification of Person Performing Review of Lab Records
- 21 CFR 211.125(f)Procedures Written and Followed
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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 |
| February 18, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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