Airgas USA, LLC

Entity profile compiled from public source records

Public Record Profile Registrations: 15 510(k) filings: 0 Recalls: 0

Known Identifiers & Locations

FEI Numbers 1000111992, 1000118364, 1033831, 1216783, 1217333, 1620065, 1946773, 2024781, 2127612, 2250062, 3007313217, 3008852974, 3008931060, 3012953378, 3024515
Owner Operator Numbers 9001096, 9005059, 9008187, 9008516, 9009904, 9027673, 9028595, 9066386
Locations Covered ATL, GA, US; BILLERICA, MA, US; Cherry Hill, NJ, US; Durham, NC, US; Elk Grove Village, IL, US; Grand Prairie, TX, US; La Porte, TX, US; SALEM, NH, US; Sacramento, CA, US; Saint Louis, MO, US; Santa Fe Spgs, CA, US; TEMPLE TERRACE, FL, US; TULSA, OK, US; Vancouver, WA, US; Waukesha, WI, US

Registered Establishments (15)

Registration # Establishment Name Location Establishment Type(s) Action
1033831 AIRGAS USA, LLC. ATL, GA, US Manufacture Medical Device View Details
1054016 Airgas USA, LLC Durham, NC, US Manufacture Medical Device View Details
1056791 AIRGAS USA, LLC. TEMPLE TERRACE, FL, US Manufacture Medical Device View Details
1217333 Airgas USA LLC BILLERICA, MA, US Manufacture Medical Device View Details
1250022 AIRGAS USA LLC SALEM, NH, US Manufacture Medical Device View Details
1620065 AIRGAS USA, LLC Grand Prairie, TX, US Manufacture Medical Device View Details
1645341 AIRGAS USA, LLC TULSA, OK, US Manufacture Medical Device View Details
1946773 Airgas USA, LLC Saint Louis, MO, US Manufacture Medical Device View Details
2024781 AIRGAS USA, LLC Santa Fe Spgs, CA, US Manufacture Medical Device View Details
2127612 AIRGAS USA LLC Waukesha, WI, US Manufacture Medical Device View Details
2250062 AIRGAS USA LLC Cherry Hill, NJ, US Manufacture Medical Device View Details
3004931173 AIRGAS USA LLC Elk Grove Village, IL, US Manufacture Medical Device View Details
3007313217 Airgas USA, LLC. La Porte, TX, US Manufacture Medical Device View Details
3008931060 Airgas USA, LLC - Sacramento Sacramento, CA, US Manufacture Medical Device View Details
3024515 AIRGAS USA, LLC Vancouver, WA, US Manufacture Medical Device View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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