FDA Inspection 1102896 — HeartStitch, Inc.

HeartStitch, Inc. — FEI 3009142291

The FDA completed an inspection of HeartStitch, Inc. on August 29, 2019 in Fountain Valley, 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
August 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fountain Valley, CA (United States)