FDA Inspection
Intelifuse IncIntelifuse Inc – FDA Inspection, Dec 23, 2009
Record Details
This FDA Inspection record concerns Intelifuse Inc, with an inspection on December 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Intelifuse Inc
- Inspection Date
- December 23, 2009
- Product Type
- Devices
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ID · ed2881c7-bd5d-467e-8433-bc8f4b430a1c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 637100
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.22Quality Audit/Reaudit - conducted
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