FDA Inspection 1232016 — Oncospace

Oncospace — FEI 3018490124

The FDA completed an inspection of Oncospace on Mar 1, 2024 in Baltimore, MD. 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
Mar 1, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)