FDA inspection

Hikma Pharmaceuticals LLC: FDA inspection ending Jul 27, 2016

FDA inspection 981353 · Voluntary Action Indicated (VAI) · Amman

Key facts

Inspection ID 981353
Firm Hikma Pharmaceuticals LLC
FEI number 3002806351
Address Baywader Wadi El-Seer, Industrial Airport Road
City Amman
Country Jordan
Fiscal year 2016
Inspection end date Jul 27, 2016
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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