FDA Inspection
Terumo Corporation Fujinomiya FactoryTerumo Corporation Fujinomiya Factory – FDA Inspection, Mar 20, 2014
Record Details
This FDA Inspection record concerns Terumo Corporation Fujinomiya Factory, with an inspection on March 20, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- March 20, 2014
- Product Type
- Drugs
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ID · 3f241b1e-852e-4ff9-a67b-5a9d34a7330b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 875358
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Terumo Corporation Fujinomiya Factory
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 19, 2023 | Not classified | Office of Inspections and Investigations | |
| February 7, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 16, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Terumo Corporation Fujinomiya Factory
- FDA Inspection 1206261 - 2023-05-19
- FDA Inspection 1004817 - 2017-02-07
- FDA Inspection 746978 - 2011-09-16
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