FDA Inspection 1204769 — BioCheck, Inc.

BioCheck, Inc. — FEI 3002564473

The FDA completed an inspection of BioCheck, Inc. on February 7, 2023 in South San Francisco, 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 7, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
South San Francisco, CA (United States)