FDA Inspection 903664 — STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD.

STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD. — FEI 3007913880

The FDA completed an inspection of STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD. on October 29, 2014 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 29, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Suzhou (China)