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FDA Import Refusal 799-7439318-3/11/1 — Johnson & Johnson K.K.

Johnson & Johnson K.K. — FEI 3004862850

The FDA refused shipment 799-7439318-3/11/1 from Johnson & Johnson K.K. (Japan) on Oct 22, 2023. The refused product falls under Devices — REPROCESSED INTRAVASCULAR ULTRASOUND CATHETER. Cited charges: 118,3280 This firm has 3 other import refusals on record.

Refusal details

Date
Oct 22, 2023
Country
Japan
Product Category
Devices
Product Code
74OWQ REPROCESSED INTRAVASCULAR ULTRASOUND CATHETER
Charges
118,3280

Other import refusals

FDA data resources

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