FDA Inspection 1244032 — Catalyst Orthoscience, Inc.

Catalyst Orthoscience, Inc. — FEI 3012552981

The FDA completed an inspection of Catalyst Orthoscience, Inc. on Jul 10, 2024 in Naples, FL. 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
Jul 10, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Naples, FL (United States)