FDA Inspection 1264613 — Mayinglong Pharmaceutical Group Co., Ltd.

Mayinglong Pharmaceutical Group Co., Ltd. — FEI 3004363818

The FDA completed an inspection of Mayinglong Pharmaceutical Group Co., Ltd. on March 14, 2025 in Wuhan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 14, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wuhan (China)

Citations

IDCFRDescription
192621 CFR 211.166(b)Adequate number of batches on stability