FDA Import Refusal 799-8111726-0/11/1 — JOHNSON & JOHNSON

JOHNSON & JOHNSON — FEI 3014477265

The FDA refused shipment 799-8111726-0/11/1 from JOHNSON & JOHNSON (Japan) on Dec 20, 2023. The refused product falls under Devices — SCALPEL, ULTRASONIC, REPROCESSED. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 20, 2023
Country
Japan
Product Category
Devices
Product Code
79NLQ SCALPEL, ULTRASONIC, REPROCESSED
Charges
118,3280,341

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