FDA Inspection 948549 — CORDIS DE MEXICO, SA DE CV

CORDIS DE MEXICO, SA DE CV — FEI 3003248396

The FDA completed an inspection of CORDIS DE MEXICO, SA DE CV on Oct 22, 2015 in Juarez. 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
Oct 22, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Juarez (Mexico)

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