FDA Inspection
Michael Steinmetz, M.D.Michael Steinmetz, M.D. – FDA Inspection, Dec 11, 2019
Record Details
This FDA Inspection record concerns Michael Steinmetz, M.D., with an inspection on December 11, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Michael Steinmetz, M.D.
- Inspection Date
- December 11, 2019
- Product Type
- Devices
View Company Profile
ID · 18fbb1a9-0991-42fe-b391-7264b4f270d6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1112329
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.150(a)(3)No investigator progress reports
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Michael Steinmetz, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 22, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Michael Steinmetz, M.D.
- FDA Inspection 1175600 - 2022-07-22
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.