FDA Inspection
Nipro Pharma Corporation - Kagamiishi PlantNipro Pharma Corporation - Kagamiishi Plant – FDA Inspection, Dec 15, 2017
Record Details
This FDA Inspection record concerns Nipro Pharma Corporation - Kagamiishi Plant, with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- Vilmary Negron Rodriguez (Issuing Officer)
View Company Profile
ID · fa457979-29d2-4f9f-87f3-330b099d3623
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1034876
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.188(b)(2)Identification of Equipment and Lines
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Other FDA inspections of Nipro Pharma Corporation - Kagamiishi Plant
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 29, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Nipro Pharma Corporation - Kagamiishi Plant
- FDA Inspection 1285960 - 2025-08-29
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