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FDA Inspection 594560 — Oscor Caribe, LLC

Oscor Caribe, LLC — FEI 3004785273

The FDA completed an inspection of Oscor Caribe, LLC on June 25, 2009 in Santo Domingo. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 25, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Santo Domingo (Dominican Republic (the))

Facility

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FDA data resources