FDA inspection

Raptim Research Pvt. Ltd.: FDA inspection ending Sep 19, 2019

FDA inspection 1110477 · No Action Indicated (NAI) · Navi Mumbai

Key facts

Inspection ID 1110477
Firm Raptim Research Pvt. Ltd.
FEI number 3007267856
Address A - 226 Near Mahape Depot
City Navi Mumbai
Country India
Fiscal year 2019
Inspection end date Sep 19, 2019
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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