# FDA Inspection 1018681 - AIRGAS USA LLC - July 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/airgas-usa-llc/ed8cbbb0-d07e-4f3d-a30a-0f7cc7d498ed
Source feed: FDA_Inspections

> FDA Inspection 1018681 for AIRGAS USA LLC on July 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018681
- Company Name: AIRGAS USA LLC
- Inspection Date: 2017-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1018681 - 2017-07-21](https://www.keypedia.com/records/fda_inspections/airgas-usa-llc/4088790e-9d99-41ed-a7a1-71eef4565f04)
- [FDA Inspection 665919 - 2010-06-09](https://www.keypedia.com/records/fda_inspections/airgas-usa-llc/c262f75d-c838-4917-b5f3-f5800048218a)
- [FDA Inspection 661335 - 2010-05-10](https://www.keypedia.com/records/fda_inspections/airgas-usa-llc/3c0000f5-25ec-4f19-8745-ccffaed53b55)

Company: https://www.keypedia.com/companies/airgas-usa-llc/1b5ff82a-12d0-4050-8856-e2f5058d986b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
