FDA Inspection
Johnson & Johnson Consumer, IncJohnson & Johnson Consumer, Inc – FDA Inspection, Aug 30, 2013
Record Details
This FDA Inspection record concerns Johnson & Johnson Consumer, Inc, with an inspection on August 30, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 30, 2013
- Product Type
- Drugs
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ID · 4600813a-603c-44ec-aeaa-75dbc49c89f1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 848116
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.63Equipment Design, Size and Location
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of Johnson & Johnson Consumer, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 24, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 27, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 9, 2010 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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