FDA Inspection 1248327 — Invivoscribe Technologies, Inc.

Invivoscribe Technologies, Inc. — FEI 3014173060

The FDA completed an inspection of Invivoscribe Technologies, Inc. on Aug 14, 2024 in San Diego, CA. 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
Aug 14, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)