FDA Inspection
The Metrix CompanyFDA Inspection 1088552 - The Metrix Company - April 25, 2019
Record Details
This FDA Inspection record concerns The Metrix Company, with an inspection on April 25, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- The Metrix Company
- Inspection Date
- April 25, 2019
- Product Type
- Devices
View Company Profile
ID · edf8a8a4-ec7d-4830-81ef-5fa8ff215df4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1088552
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of The Metrix Company
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 6, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 9, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 22, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for The Metrix Company
- FDA Inspection 969394 - 2016-05-06
- FDA Inspection 886826 - 2014-07-09
- FDA Inspection 662262 - 2010-04-22
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.