FDA inspection

Cadila Pharmaceuticals Limited: FDA inspection ending Sep 26, 2025

FDA inspection 1293740 · No Action Indicated (NAI) · Ahmedabad

Key facts

Inspection ID 1293740
Firm Cadila Pharmaceuticals Limited
FEI number 3007684569
Address 1389 Trasad Road, Dholka
City Ahmedabad
Country India
Fiscal year 2025
Inspection end date Sep 26, 2025
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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