FDA Inspection
Tri-Tech Manufacturing IncTri-Tech Manufacturing Inc – FDA Inspection, Dec 6, 2012
Record Details
This FDA Inspection record concerns Tri-Tech Manufacturing Inc, with an inspection on December 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Tri-Tech Manufacturing Inc
- Inspection Date
- December 6, 2012
- Product Type
- Devices
View Company Profile
ID · 8875c519-d7b6-489b-bf8d-c736c6cf7f45
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 810408
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Tri-Tech Manufacturing Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 3, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 13, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 8, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Tri-Tech Manufacturing Inc
- FDA Inspection 938455 - 2015-08-13
- FDA Inspection 921300 - 2015-04-03
- FDA Inspection 848794 - 2013-09-13
- FDA Inspection 674396 - 2010-06-08
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