FDA Inspection 682281 — Exsilent Usa, Llc

Exsilent Usa, Llc — FEI 3008484254

The FDA completed an inspection of Exsilent Usa, Llc on Sep 8, 2010 in Eden Prairie, MN. 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
Sep 8, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Eden Prairie, MN (United States)