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FDA Inspection
•Transamerican Technologies International•May 4, 2018

Transamerican Technologies International – FDA Inspection, May 4, 2018

Record Details

This FDA Inspection record concerns Transamerican Technologies International, with an inspection on May 4, 2018, issued by the San Francisco District Office, covering medical devices & rad health.

Company
Transamerican Technologies International
Inspection Date
May 4, 2018
Product Type
Medical Devices & Rad Health
Office
San Francisco District Office
Person
  • Maida Henesian (Company Rep)
View Company Profile

ID · 4c13519b-6546-456f-ba59-39fd4958bb12

Inspection Facts

Inspection number
1052422
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Transamerican Technologies International

4
DateClassificationOfficeProject area
July 22, 2026VAICenter for Devices and Radiological HealthCompliance: Devices
March 26, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 27, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 23, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Transamerican Technologies International
  • FDA Inspection 1327408 - 2026-07-22
  • FDA Inspection 920409 - 2015-03-26
  • FDA Inspection 820406 - 2013-02-27
  • FDA Inspection 698617 - 2010-11-23

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