FDA Inspection 1114423 — Oscor Caribe, LLC

Oscor Caribe, LLC — FEI 3004785273

The FDA completed an inspection of Oscor Caribe, LLC on Dec 11, 2019 in Santo Domingo. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 11, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Santo Domingo (Dominican Republic (the))

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.