FDA Inspection
Xinjiang Nuziline Biopharmaceutical Co., Ltd.Xinjiang Nuziline Biopharmaceutical Co., Ltd. – FDA Inspection, Nov 11, 2016
Record Details
This FDA Inspection record concerns Xinjiang Nuziline Biopharmaceutical Co., Ltd., with an inspection on November 11, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 11, 2016
- Product Type
- Drugs
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ID · 7f75724a-9e4e-4f2d-8918-4b8052622403
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 998358
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
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