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FDA Inspection
•Teco Diagnostics, Inc.•October 14, 2011

Teco Diagnostics, Inc. – FDA Inspection, Oct 14, 2011

Record Details

This FDA Inspection record concerns Teco Diagnostics, Inc., with an inspection on October 14, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Teco Diagnostics, Inc.
Inspection Date
October 14, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 8cc7bffd-30cd-4236-9df9-2a7ddde902f0

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
753658
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Teco Diagnostics, Inc.

5
DateClassificationOfficeProject area
February 5, 2026Not classifiedLos Angeles District Office
October 27, 2021NAICenter for Devices and Radiological HealthCompliance: Devices
May 9, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
April 4, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
April 26, 2010OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Teco Diagnostics, Inc.
  • FDA Inspection 1309600 - 2026-02-05
  • FDA Inspection 1156041 - 2021-10-27
  • FDA Inspection 1052273 - 2018-05-09
  • FDA Inspection 831948 - 2013-04-04
  • FDA Inspection 660426 - 2010-04-26

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