FDA Inspection 1235581 — Scinopharm Taiwan, Ltd.

Scinopharm Taiwan, Ltd. — FEI 3002840477

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