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FDA Inspection 809441 — Cardiva Medical, Inc.

Cardiva Medical, Inc. — FEI 3015145497

The FDA completed an inspection of Cardiva Medical, Inc. on November 19, 2012 in Santa Clara, 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
November 19, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Clara, CA (United States)

Facility

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FDA data resources