FDA Inspection 1236240 — Sunshine Lake Pharma Co., Ltd

Sunshine Lake Pharma Co., Ltd — FEI 3007721552

The FDA completed an inspection of Sunshine Lake Pharma Co., Ltd on March 22, 2024 in Dongguan. 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
March 22, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dongguan (China)