FDA Inspection 933588 — SUZUKEN CO., LTD. OGUCHI CENTER

SUZUKEN CO., LTD. OGUCHI CENTER — FEI 3006540105

The FDA completed an inspection of SUZUKEN CO., LTD. OGUCHI CENTER on June 17, 2015 in Niwa-Gun. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 17, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Niwa-Gun (Japan)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures