FDA Inspection 1339660 — Aero-Med LLC

Aero-Med LLC — FEI 3006191977

The FDA completed an inspection of Aero-Med LLC on Oct 1, 2026 in East Hartford, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 1, 2026
Fiscal Year
2027
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
East Hartford, CT (United States)