FDA Inspection 942011 — Bittium Biosignals Ltd.

Bittium Biosignals Ltd. — FEI 1000425315

The FDA completed an inspection of Bittium Biosignals Ltd. on July 16, 2015 in Kuopio. 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 16, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Kuopio (Finland)