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FDA Inspection
•Tri-Tech Manufacturing Inc•September 13, 2013

Tri-Tech Manufacturing Inc – FDA Inspection, Sep 13, 2013

Record Details

This FDA Inspection record concerns Tri-Tech Manufacturing Inc, with an inspection on September 13, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Tri-Tech Manufacturing Inc
Inspection Date
September 13, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · d409b37a-e82e-4c46-9501-6845ca2ac467

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
848794
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Tri-Tech Manufacturing Inc

4
DateClassificationOfficeProject area
August 13, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
April 3, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
December 6, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
June 8, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Tri-Tech Manufacturing Inc
  • FDA Inspection 938455 - 2015-08-13
  • FDA Inspection 921300 - 2015-04-03
  • FDA Inspection 810408 - 2012-12-06
  • FDA Inspection 674396 - 2010-06-08

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