FDA Inspection
Hoodman CorporationHoodman Corporation – FDA Inspection, Mar 31, 2011
Record Details
This FDA Inspection record concerns Hoodman Corporation, with an inspection on March 31, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hoodman Corporation
- Inspection Date
- March 31, 2011
- Product Type
- Devices
View Company Profile
ID · 36fe5390-adc9-4f7b-a799-fb9b63a41c52
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 726582
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(a)Production processes
- 21 CFR 820.22Quality Audit/Reaudit - conducted
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Other FDA inspections of Hoodman Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 9, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hoodman Corporation
- FDA Inspection 657966 - 2010-04-09
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