FDA Inspection 900838 — SMITH & NEPHEW ORTHOPEDICS (BEIJING) CO., LTD.

SMITH & NEPHEW ORTHOPEDICS (BEIJING) CO., LTD. — FEI 3008892118

The FDA completed an inspection of SMITH & NEPHEW ORTHOPEDICS (BEIJING) CO., LTD. on Sep 11, 2014 in Tongzhou District. 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
Sep 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Tongzhou District (China)