FDA Inspection 1088940 — Alung Technologies Inc

Alung Technologies Inc — FEI 3009763347

The FDA completed an inspection of Alung Technologies Inc on April 3, 2019 in Pittsburgh, PA. 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
April 3, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Pittsburgh, PA (United States)