FDA Inspection
M&M Innovations, Inc.M&M Innovations, Inc. – FDA Inspection, Nov 2, 2016
Record Details
This FDA Inspection record concerns M&M Innovations, Inc., with an inspection on November 2, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ef428afe-88ed-42fe-b2e8-df016ed535d7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 997027
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
6- 21 CFR 211.84(d)(1)Component identity verification
- 21 CFR 211.101(d)Component release checked by 2nd person
- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.28(b)Habits of good sanitation & health
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.42(c)(5)Mfg / Processing Operations Area
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Other FDA inspections of M&M Innovations, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2022 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| December 15, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for M&M Innovations, Inc.
- FDA Inspection 1170472 - 2022-05-12
- FDA Inspection 703593 - 2010-12-15
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