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FDA Import Refusal 799-6200120-9/11/1A — AGM OVERSEAS

AGM OVERSEAS — FEI 3014419623

The FDA refused shipment 799-6200120-9/11/1A from AGM OVERSEAS (India) on Jun 25, 2018. The refused product falls under Devices — STATIONARY ULTRASONIC DIATHERMY DEVICE FOR USE IN APPLYING THERAPEUTIC DEEP HEAT. Cited charges: 118,3280,508

Refusal details

Date
Jun 25, 2018
Country
India
Product Category
Devices
Product Code
89PFW STATIONARY ULTRASONIC DIATHERMY DEVICE FOR USE IN APPLYING THERAPEUTIC DEEP HEAT
Charges
118,3280,508

FDA data resources

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