FDA Inspection 1266993 — Nanjing Clinical Tech Laboratories Inc.

Nanjing Clinical Tech Laboratories Inc. — FEI 3019762892

The FDA completed an inspection of Nanjing Clinical Tech Laboratories Inc. on Oct 18, 2024 in Nanjing. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 18, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Nanjing (China)

Additional Details

Bioanalytical BA/BE

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.