FDA Inspection 1198299 — MicroPort Orthopedics Inc.

MicroPort Orthopedics Inc. — FEI 3010536692

The FDA completed an inspection of MicroPort Orthopedics Inc. on Feb 8, 2023 in Arlington, TN. 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
Feb 8, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Arlington, TN (United States)