FDA Inspection 1153168 — Jie Li

Jie Li — FEI 3019043088

The FDA completed an inspection of Jie Li on July 30, 2021 in Beijing. 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
July 30, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Beijing (China)

Additional Details

Clinical Investigator (CI)