FDA Inspection 837943 — Alphatek Corp

Alphatek Corp — FEI 1419225

The FDA completed an inspection of Alphatek Corp on July 2, 2013 in Broadview, IL. 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
July 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Broadview, IL (United States)