FDA Inspection 1273595 — Raybow (Suzhou) Pharmaceutical Co., Ltd.

Raybow (Suzhou) Pharmaceutical Co., Ltd. — FEI 3007114474

The FDA completed an inspection of Raybow (Suzhou) Pharmaceutical Co., Ltd. on May 22, 2025 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 22, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Suzhou (China)