FDA Inspection
Interrad Medical IncInterrad Medical Inc – FDA Inspection, Jul 31, 2014
Record Details
This FDA Inspection record concerns Interrad Medical Inc, with an inspection on July 31, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Interrad Medical Inc
- Inspection Date
- July 31, 2014
- Product Type
- Devices
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ID · 23d9f7a4-2432-4b66-904f-a3766f6b3f3e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 889005
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.30(b)Design plans - Lack of or inadequate
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Other FDA inspections of Interrad Medical Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Interrad Medical Inc
- FDA Inspection 699977 - 2010-11-05
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