FDA Inspection
Zolberg CorporationZolberg Corporation – FDA Inspection, May 5, 2017
Record Details
This FDA Inspection record concerns Zolberg Corporation, with an inspection on May 5, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 78ddc1f2-ea2d-41c8-848f-f163f2f1a6ec
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1013378
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zolberg Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 7, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 23, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zolberg Corporation
- FDA Inspection 1227151 - 2023-12-07
- FDA Inspection 776050 - 2012-03-23
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