FDA Inspection 1268116 — Guangxi Yulin Pharmaceutical Group Co. Ltd.

Guangxi Yulin Pharmaceutical Group Co. Ltd. — FEI 1000589993

The FDA completed an inspection of Guangxi Yulin Pharmaceutical Group Co. Ltd. on Mar 21, 2025 in Yulin. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 21, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yulin (China)

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