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FDA Inspection
•AIRGAS USA LLC•July 21, 2017

AIRGAS USA LLC – FDA Inspection, Jul 21, 2017

Record Details

This FDA Inspection record concerns AIRGAS USA LLC, with an inspection on July 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
AIRGAS USA LLC
Inspection Date
July 21, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Karen M. Cruz Arenas (Issuing Officer)
View Company Profile

ID · ed8cbbb0-d07e-4f3d-a30a-0f7cc7d498ed

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1018681
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

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

Full citation text and observation details available on the Dashboard.

Other FDA inspections of AIRGAS USA LLC

2
DateClassificationOfficeProject area
June 9, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 10, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for AIRGAS USA LLC
  • FDA Inspection 665919 - 2010-06-09
  • FDA Inspection 661335 - 2010-05-10

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