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FDA Inspection
•Air Techniques Inc•August 20, 2012

Air Techniques Inc – FDA Inspection, Aug 20, 2012

Record Details

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

Company
Air Techniques Inc
Inspection Date
August 20, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c15fd3fb-153d-4b65-a6a3-29e3ce233616

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
795593
FDA center
Medical Devices & Rad Health
Project area
Radiation Control and Health Safety Act

FDA Citations

4
  1. 21 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))
  2. 21 CFR 820.198(a)Complaints
  3. 21 CFR 820.100(b)Documentation
  4. 21 CFR 820.30(d)Design output - Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Air Techniques Inc

5
DateClassificationOfficeProject area
June 6, 2019NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
October 19, 2016NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
April 29, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
September 12, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 5, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Air Techniques Inc
  • FDA Inspection 1115251 - 2019-06-06
  • FDA Inspection 989060 - 2016-10-19
  • FDA Inspection 969945 - 2016-04-29
  • FDA Inspection 896921 - 2014-09-12
  • FDA Inspection 651132 - 2010-02-05

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