FDA Inspection
Hatten Paul MDHatten Paul MD – FDA Inspection, Feb 24, 2009
Record Details
This FDA Inspection record concerns Hatten Paul MD, with an inspection on February 24, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hatten Paul MD
- Inspection Date
- February 24, 2009
- Product Type
- Devices
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ID · 82c3d5b4-8fd9-445c-893b-739590455170
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 568143
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 50.27(a)Consent form not approved/signed/dated
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