FDA Inspection
Airgas USA, LLCAirgas USA, LLC – FDA Inspection, Oct 16, 2015
Record Details
This FDA Inspection record concerns Airgas USA, LLC, with an inspection on October 16, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Airgas USA, LLC
- Inspection Date
- October 16, 2015
- Product Type
- Devices
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ID · 5ff17b82-b681-4196-8f00-e9a27ba3beb3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 953766
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Airgas USA, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 31, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Airgas USA, LLC
- FDA Inspection 1099562 - 2019-07-31
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