FDA Inspection 1097252 — Raptim Research Pvt. Ltd.

Raptim Research Pvt. Ltd. — FEI 3007267856

The FDA completed an inspection of Raptim Research Pvt. Ltd. on May 29, 2019 in Navi Mumbai. 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
May 29, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Navi Mumbai (India)

Additional Details

Clinical BA/BE

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