FDA Inspection 917104 — Airistar Technologies LLC

Airistar Technologies LLC — FEI 3005583594

The FDA completed an inspection of Airistar Technologies LLC on March 3, 2015 in Waukegan, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 3, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Waukegan, IL (United States)