FDA Inspection 1231392 — Bioport Korea Inc.

Bioport Korea Inc. — FEI 3010280072

The FDA completed an inspection of Bioport Korea Inc. on Mar 7, 2024 in Yangsan. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Yangsan (Korea (the Republic of))

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