FDA Inspection
Goldman, Mitchel P MDGoldman, Mitchel P MD – FDA Inspection, Aug 24, 2012
Record Details
This FDA Inspection record concerns Goldman, Mitchel P MD, with an inspection on August 24, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Goldman, Mitchel P MD
- Inspection Date
- August 24, 2012
- Product Type
- Devices
View Company Profile
ID · 74c048ae-c1b9-46a7-bb34-5d476af0f5d0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 796672
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(2)(i)Investigator device accountability inadequate
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Goldman, Mitchel P MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 12, 2009 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Goldman, Mitchel P MD
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.