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FDA Inspection
•Theg, Inc.•June 20, 2012

Theg, Inc. – FDA Inspection, Jun 20, 2012

Record Details

This FDA Inspection record concerns Theg, Inc., with an inspection on June 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Theg, Inc.
Inspection Date
June 20, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c2e1c784-15a3-4478-aa42-a68a51871990

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
791127
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Theg, Inc.

3
DateClassificationOfficeProject area
August 16, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
November 15, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
October 13, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Theg, Inc.
  • FDA Inspection 1026149 - 2017-08-16
  • FDA Inspection 857464 - 2013-11-15
  • FDA Inspection 620022 - 2009-10-13

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