FDA Inspection 1086589 — Biofermin Pharmaceutical Co., Ltd. Kobe Plant

Biofermin Pharmaceutical Co., Ltd. Kobe Plant — FEI 3013222283

The FDA completed an inspection of Biofermin Pharmaceutical Co., Ltd. Kobe Plant on Jan 25, 2019 in Kobe. 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
Jan 25, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Kobe (Japan)

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