FDA Inspection 1086603 — Hepatiq, Inc.

Hepatiq, Inc. — FEI 3011527394

The FDA completed an inspection of Hepatiq, Inc. on March 7, 2019 in Irvine, 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
March 7, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)