FDA Inspection
Joyang LaboratoriesJoyang Laboratories – FDA Inspection, May 5, 2017
Record Details
This FDA Inspection record concerns Joyang Laboratories, with an inspection on May 5, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ba24452a-e8bc-4f52-88f5-faa9caf0baf2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1021129
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Joyang Laboratories
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 25, 2025 | Not classified | Office of Inspections and Investigations | |
| August 22, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Joyang Laboratories
- FDA Inspection 1268707 - 2025-04-25
- FDA Inspection 1135083 - 2019-08-22
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