FDA inspection

OSKO, Inc.: FDA inspection ending Aug 17, 2017

FDA inspection 1022321 · Voluntary Action Indicated (VAI) · Medley, FL

Key facts

Inspection ID 1022321
Firm OSKO, Inc.
FEI number 3010666400
Address 8085 Nw 90th St
City Medley
State FL
ZIP 33166
Country United States
Fiscal year 2017
Inspection end date Aug 17, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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