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FDA Inspection 1099927 — Seikagaku Corporation

Seikagaku Corporation — FEI 1000255210

The FDA completed an inspection of Seikagaku Corporation on Jul 19, 2019 in Takahagi. 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
Jul 19, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Takahagi (Japan)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.