FDA Inspection
Master Herbs, Inc.Master Herbs, Inc. – FDA Inspection, Sep 14, 2020
Record Details
This FDA Inspection record concerns Master Herbs, Inc., with an inspection on September 14, 2020, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Master Herbs, Inc.
- Inspection Date
- September 14, 2020
- Product Type
- Drugs
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ID · e346ab91-9368-4e1b-aca3-15e10b65fddd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1129151
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.142(b)Storage under appropriate conditions
- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 211.22(a)Contract drug products--lack of responsibility
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Master Herbs, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2019 | Not classified | Los Angeles District Office | Drug Quality Assurance |
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