FDA Inspection 1269495 — Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.

Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. — FEI 3004268442

The FDA completed an inspection of Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. on April 11, 2025 in Nanning. 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
April 11, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nanning (China)