FDA Inspection
Daniel Nader, DODaniel Nader, DO – FDA Inspection, Apr 17, 2012
Record Details
This FDA Inspection record concerns Daniel Nader, DO, with an inspection on April 17, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Daniel Nader, DO
- Inspection Date
- April 17, 2012
- Product Type
- Devices
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ID · 8e5c3050-55b4-49ec-af60-816f69f0551e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 777222
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
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