FDA Inspection 1021517 — Multivitamin Direct Inc.
The FDA completed an inspection of Multivitamin Direct Inc. on August 10, 2017 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 4 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 10, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- San Jose, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15459 | 21 CFR 111.20(d) | Physical plant - design and construction |
| 15763 | 21 CFR 111.205(a) | Master manufacturing record - unique formulation |
| 15951 | 21 CFR 111.110(c) | Quality control operations - tests, examinations; results |
| 15978 | 21 CFR 111.123(a)(2) | Quality control operations - batch production records |