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FDA Inspection
•Patterson Technology Center, Inc.•September 29, 2017

Patterson Technology Center, Inc. – FDA Inspection, Sep 29, 2017

Record Details

This FDA Inspection record concerns Patterson Technology Center, Inc., with an inspection on September 29, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Patterson Technology Center, Inc.
Inspection Date
September 29, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Mary A. Millner
View Company Profile

ID · 1e3c164c-a4d5-40f7-b2a8-9966c7aa5261

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1027046
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.100(a)Lack of or inadequate procedures
  2. 21 CFR 820.198(a)Lack of or inadequate complaint procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Patterson Technology Center, Inc.

2
DateClassificationOfficeProject area
April 17, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 8, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Patterson Technology Center, Inc.
  • FDA Inspection 777336 - 2012-04-17
  • FDA Inspection 656540 - 2010-04-08

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