FDA Inspection 818869 — BioCardia, Inc.

BioCardia, Inc. — FEI 3003610571

The FDA completed an inspection of BioCardia, Inc. on February 14, 2013 in Sunnyvale, CA. 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
February 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)