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FDA Import Refusal AEK-2357894-8/1/1 — Philips

Philips — FEI 3003799836

The FDA refused shipment AEK-2357894-8/1/1 from Philips (Netherlands) on Aug 23, 2016. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charges: 118,341 This firm has 3 other import refusals on record.

Refusal details

Date
Aug 23, 2016
Country
Netherlands
Product Category
Devices
Product Code
90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
Charges
118,341

Other import refusals

FDA data resources

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