FDA inspection

Protalix Ltd.: FDA inspection ending Jul 11, 2019

FDA inspection 1100788 · No Action Indicated (NAI) · Karmi'El

Key facts

Inspection ID 1100788
Firm Protalix Ltd.
FEI number 3008289067
Address Science Park, 2, Snunit Street
City Karmi'El
Country Israel
Fiscal year 2019
Inspection end date Jul 11, 2019
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
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
  • 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

Browse all FDA inspections