FDA Inspection 767900 — Alken Inc.

Alken Inc. — FEI 1000246715

The FDA completed an inspection of Alken Inc. on February 16, 2012 in Colchester, VT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 16, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Colchester, VT (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained