FDA Inspection 1235581 — Scinopharm Taiwan, Ltd.

Scinopharm Taiwan, Ltd. — FEI 3002840477

The FDA completed an inspection of Scinopharm Taiwan, Ltd. on Mar 21, 2024 in Tainan City. 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
Mar 21, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Tainan City (Taiwan)

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