FDA Inspection 1027428 — Alken Inc.

Alken Inc. — FEI 1000246715

The FDA completed an inspection of Alken Inc. on September 12, 2017 in Colchester, VT. 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
September 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Colchester, VT (United States)