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FDA Inspection
•Airgas USA, LLC•April 10, 2012

Airgas USA, LLC – FDA Inspection, Apr 10, 2012

Record Details

This FDA Inspection record concerns Airgas USA, LLC, with an inspection on April 10, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Airgas USA, LLC
Inspection Date
April 10, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · e096af9b-fbc2-462b-8da9-572e54d2e18a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
777381
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

4
  1. 21 CFR 820.25(a)Personnel
  2. 21 CFR 820.75(a)Documentation
  3. 21 CFR 820.20(b)Lack of or inadequate organizational structure
  4. 21 CFR 803.17(a)(1)Lack of System for Event Evaluations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Airgas USA, LLC

3
DateClassificationOfficeProject area
December 22, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
October 28, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 14, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Airgas USA, LLC
  • FDA Inspection 960314 - 2015-12-22
  • FDA Inspection 904861 - 2014-10-28
  • FDA Inspection 666436 - 2010-05-14

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