FDA Inspection
Integra MicrofranceIntegra Microfrance – FDA Inspection, Sep 12, 2013
Record Details
This FDA Inspection record concerns Integra Microfrance, with an inspection on September 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Integra Microfrance
- Inspection Date
- September 12, 2013
- Product Type
- Devices
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ID · ca4fdb80-5199-4f32-8e0b-7bd503b68102
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 857175
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.184Lack of or inadequate DHR procedures
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Other FDA inspections of Integra Microfrance
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 18, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Integra Microfrance
- FDA Inspection 959800 - 2016-02-18
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