FDA Inspection 804647 — Apollo Corp

Apollo Corp — FEI 2182947

The FDA completed an inspection of Apollo Corp on October 24, 2012 in Somerset, WI. 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
October 24, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Somerset, WI (United States)