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FDA Import Refusal 799-2253798-7/11/1 — ENTERMED BV

ENTERMED BV — FEI 3013733547

The FDA refused shipment 799-2253798-7/11/1 from ENTERMED BV (Netherlands) on Sep 28, 2017. The refused product falls under Devices — LIGHT, EXAMINATION, MEDICAL, BATTERY POWERED. Cited charge: 3280

Refusal details

Date
Sep 28, 2017
Country
Netherlands
Product Category
Devices
Product Code
80KYT LIGHT, EXAMINATION, MEDICAL, BATTERY POWERED
Charges
3280

FDA data resources

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