FDA Inspection 1173908 — Inbios

Inbios — FEI 3021502848

The FDA completed an inspection of Inbios on Jun 15, 2022 in Seattle, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 15, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Seattle, WA (United States)