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FDA Inspection 841836 — Oscor Caribe, LLC

Oscor Caribe, LLC — FEI 3004785273

The FDA completed an inspection of Oscor Caribe, LLC on July 25, 2013 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
July 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Santo Domingo (Dominican Republic (the))

Facility

Other inspections at this facility

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  • 1199358 (NAI Wed Jan 18 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114423 (NAI Wed Dec 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 749326 (VAI Fri Aug 19 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 594560 (VAI Thu Jun 25 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources