FDA Inspection
Walter F. KerwinWalter F. Kerwin – FDA Inspection, Jan 27, 2010
Record Details
This FDA Inspection record concerns Walter F. Kerwin, with an inspection on January 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Walter F. Kerwin
- Inspection Date
- January 27, 2010
- Product Type
- Devices
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ID · c31da65f-170b-40ad-8289-472ed45b11d4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 649487
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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