FDA Inspection
Shenzhen Oriental Pharmaceutical Co LtdShenzhen Oriental Pharmaceutical Co Ltd – FDA Inspection, Jan 11, 2019
Record Details
This FDA Inspection record concerns Shenzhen Oriental Pharmaceutical Co Ltd, with an inspection on January 11, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · a3857e9b-ef9d-45e0-8bf3-00a592e74f77
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1080368
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Shenzhen Oriental Pharmaceutical Co Ltd
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 29, 2024 | Not classified | Office of Inspections and Investigations | |
| June 7, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 20, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shenzhen Oriental Pharmaceutical Co Ltd
- FDA Inspection 1258257 - 2024-11-29
- FDA Inspection 976107 - 2016-06-07
- FDA Inspection 872742 - 2014-03-20
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