FDA Import Refusal 799-6907113-3/11/1 — Johnson & Johnson Consumer Company
The FDA refused shipment 799-6907113-3/11/1 from Johnson & Johnson Consumer Company (Japan) on Oct 23, 2023. The refused product falls under Devices — SCALPEL, ULTRASONIC, REPROCESSED. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Oct 23, 2023
- Country
- Japan
- Product Category
- Devices
- Product Code
- 79NLQ SCALPEL, ULTRASONIC, REPROCESSED
- Charges
- 118,3280