FDA inspection

Oscor Caribe, LLC: FDA inspection ending Jun 25, 2009

FDA inspection 594560 · Voluntary Action Indicated (VAI) · Santo Domingo

Key facts

Inspection ID 594560
Firm Oscor Caribe, LLC
FEI number 3004785273
Address Zona Franca Las Americas, Nave I-2, Autopista Las Americas Km 22
City Santo Domingo
Country Dominican Republic (the)
Fiscal year 2009
Inspection end date Jun 25, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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