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FDA Inspection 825404 — Terumo Medical Products (Hangzhou) Co., Ltd.

Terumo Medical Products (Hangzhou) Co., Ltd. — FEI 3004102031

The FDA completed an inspection of Terumo Medical Products (Hangzhou) Co., Ltd. on March 21, 2013 in Hangzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)

Citations

IDCFRDescription
79321 CFR 803.53(a)Failure to Submit 5 Day Report

Facility

Other inspections at this facility

  • 1062256 (NAI Wed Jul 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 948623 (NAI Thu Oct 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 761927 (OAI Fri Dec 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources