FDA Inspection 1281156 — Raptim Research Pvt. Ltd.

Raptim Research Pvt. Ltd. — FEI 3007267856

The FDA completed an inspection of Raptim Research Pvt. Ltd. on Jul 25, 2025 in Navi Mumbai. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jul 25, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Navi Mumbai (India)

Additional Details

Bioanalytical BA/BE

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