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FDA Inspection
•Tenacore Holdings, Inc•August 22, 2018

FDA Inspection 1066010 - Tenacore Holdings, Inc - August 22, 2018

Record Details

This FDA Inspection record concerns Tenacore Holdings, Inc, with an inspection on August 22, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Tenacore Holdings, Inc
Inspection Date
August 22, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 1bd79fd9-585d-457e-a6fd-590e8dfa5c3e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1066010
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Tenacore Holdings, Inc

1
DateClassificationOfficeProject area
August 8, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Tenacore Holdings, Inc
  • FDA Inspection 890579 - 2014-08-08

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