FDA Inspection 1270490 — Kai Huang

Kai Huang — FEI 3033281718

The FDA completed an inspection of Kai Huang on May 16, 2025 in Wuxi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wuxi (China)

Additional Details

Clinical BA/BE