FDA inspection

Zydus Lifesciences Limited: FDA inspection ending Aug 24, 2018

FDA inspection 1066839 · No Action Indicated (NAI) · Ahmedabad

Key facts

Inspection ID 1066839
Firm Zydus Lifesciences Limited
FEI number 3012977526
Address Plot Survey 23,25/P,37,40/P,42 To 47, Ramdev Masala, Sarkhej-Bavla N.H. 8a, Tal Sanand
City Ahmedabad
Fiscal year 2018
Inspection end date Aug 24, 2018
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Generic Drug Evaluation|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices
Product type Devices, Drugs

At a glance

  • None Citations
  • None 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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