FDA Inspection
Osteometer MediTech IncOsteometer MediTech Inc – FDA Inspection, Feb 19, 2016
Record Details
This FDA Inspection record concerns Osteometer MediTech Inc, with an inspection on February 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Osteometer MediTech Inc
- Inspection Date
- February 19, 2016
- Product Type
- Devices
View Company Profile
ID · a6bf5dc3-d262-47b0-abfb-72e8b554de8c
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 989319
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Osteometer MediTech Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 9, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 8, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Osteometer MediTech Inc
- FDA Inspection 854160 - 2013-09-09
- FDA Inspection 612808 - 2009-07-08
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.