FDA inspection

ApiFix, Ltd.: FDA inspection ending Jun 6, 2019

FDA inspection 1092360 · Voluntary Action Indicated (VAI) · Yokneam Elit

Key facts

Inspection ID 1092360
Firm ApiFix, Ltd.
FEI number 3013461531
Address Misgav Business Park, 17, Tehelet St.
City Yokneam Elit
Country Israel
Fiscal year 2019
Inspection end date Jun 6, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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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