FDA Import Refusal 799-3007740-9/11/1 — KISHIYA INC

KISHIYA INC — FEI 3016925081

The FDA refused shipment 799-3007740-9/11/1 from KISHIYA INC (Japan) on Feb 7, 2023. The refused product falls under Devices — CATHETER, BALLOON TYPE. Cited charges: 118,3280

Refusal details

Date
Feb 7, 2023
Country
Japan
Product Category
Devices
Product Code
79GBA CATHETER, BALLOON TYPE
Charges
118,3280

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