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FDA Import Refusal AEK-7411918-9/10002/1 — AVISH JAISWAR

AVISH JAISWAR — FEI 3038809310

The FDA refused shipment AEK-7411918-9/10002/1 from AVISH JAISWAR (India) on Sep 23, 2025. The refused product falls under Devices — ENDOSCOPE, TRANSCERVICAL (AMNIOSCOPE)(AND ACCESSORIES). Cited charges: 118,3280,341,508

Refusal Details

Date
Sep 23, 2025
Country
India
Product Category
Devices
Product Code
85HEZ ENDOSCOPE, TRANSCERVICAL (AMNIOSCOPE)(AND ACCESSORIES)
Charges
118,3280,341,508

FDA data resources

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