FDA Inspection 1038530 — Pusadee Suchinda

Pusadee Suchinda — FEI 3013891702

The FDA completed an inspection of Pusadee Suchinda on Jan 11, 2018 in Sumter, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 11, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sumter, SC (United States)

Additional Details

Clinical Investigator (CI)

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