FDA Import Refusal 799-4550573-5/20002/1A — Ktr Europe Gmbh
The FDA refused shipment 799-4550573-5/20002/1A from Ktr Europe Gmbh (Germany) on Nov 13, 2025. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,3280,3904,3905,508 This firm has 2 other import refusals on record.
Refusal Details
- Date
- Nov 13, 2025
- Country
- Germany
- Product Category
- Devices
- Product Code
- 80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
- Charges
- 118,3280,3904,3905,508