FDA Inspection 1085327 — Samsung Bioepis Co., Ltd.

Samsung Bioepis Co., Ltd. — FEI 3010031951

The FDA completed an inspection of Samsung Bioepis Co., Ltd. on Feb 15, 2019 in Yeonsu. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yeonsu (Korea (the Republic of))

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