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FDA Import Refusal AEK-0854210-9/1/1 — Megstrumentazione

Megstrumentazione — FEI 3009895419

The FDA refused shipment AEK-0854210-9/1/1 from Megstrumentazione (Italy) on Mar 24, 2015. The refused product falls under Devices — STIMULATOR, MUSCLE, POWERED. Cited charges: 118,3280

Refusal details

Date
Mar 24, 2015
Country
Italy
Product Category
Devices
Product Code
89IPF STIMULATOR, MUSCLE, POWERED
Charges
118,3280

FDA data resources

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