FDA Import Refusal AEK-9198871-5/70003/1 — MERZ AESTHETICS
The FDA refused shipment AEK-9198871-5/70003/1 from MERZ AESTHETICS (Brazil) on Dec 11, 2025. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Dec 11, 2025
- Country
- Brazil
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 75