FDA Inspection
Viamco, Inc.Viamco, Inc. – FDA Inspection, Jan 29, 2026
Record Details
This FDA Inspection record concerns Viamco, Inc., with an inspection on January 29, 2026, issued by the San Francisco District Office, covering foods & cosmetics.
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ID · 74bffee2-5020-4ea4-8c01-9bc6aaa6e1e3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1300348
- FDA center
- Foods & Cosmetics
- Project area
- Food Composition, Standards, Labeling, and Economics
- Outcome
- Form 483 issued
FDA Citations
7- 21 CFR 111.103Written procedures - follow; quality control operations
- 21 CFR 111.205(a)Master manufacturing record - prepared
- 21 CFR 111.260Batch record - required information
- 21 CFR 111.70(b)Specifications - components
- 21 CFR 111.70(e)Specifications - finished dietary supplement
- 21 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
- 21 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
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Other FDA inspections of Viamco, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 20, 2017 | VAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
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