FDA Inspection 837673 — Femcap, Inc.

Femcap, Inc. — FEI 3002764647

The FDA completed an inspection of Femcap, Inc. on June 26, 2013 in Warren, MI. 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
June 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Warren, MI (United States)