FDA Inspection
KUNBO COMPANYFDA Inspection 1248501 - KUNBO COMPANY - September 06, 2024
Record Details
This FDA Inspection record concerns KUNBO COMPANY, with an inspection on September 6, 2024, issued by the Office of Inspections and Investigations, covering foods & cosmetics.
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ID · b9cdf098-3d02-4a85-a18a-2c830f24acde
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1248501
- FDA center
- Foods & Cosmetics
- Project area
- Foodborne Biological Hazards
- Outcome
- Form 483 issued
FDA Citations
14- 21 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
- 21 CFR 114.100(b)Maintenance of processing and production records
- 21 CFR 114.80(a)(4)Container testing
- 21 CFR 114.80(a)(2)pH testing
- 21 CFR 111.210Master manufacturing record - record requirements
- 21 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
- 21 CFR 111.105(b)Quality control - supplier qualification
- 21 CFR 111.260Batch record - required information
- 21 CFR 114.80(b)Code - required elements
- 21 CFR 111.70(b)Specifications - components
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