FDA inspection

Ajanta Pharma Ltd.: FDA inspection ending Jun 28, 2019

FDA inspection 1097061 · Voluntary Action Indicated (VAI) · Paithan

Key facts

Inspection ID 1097061
Firm Ajanta Pharma Ltd.
FEI number 3006785788
Address B-4/5/6 MIDC Industrial Area, Paithan
City Paithan
Country India
Fiscal year 2019
Inspection end date Jun 28, 2019
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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