FDA Import Refusal AEK-1274395-9/11/1 — Avanos Medical, Inc.
The FDA refused shipment AEK-1274395-9/11/1 from Avanos Medical, Inc. (United States) on June 14, 2022. The refused product falls under Devices — GENERATOR, LESION, RADIOFREQUENCY. Cited charge: 118
Refusal Details
- Date
- June 14, 2022
- Country
- United States
- Product Category
- Devices
- Product Code
- 84GXD GENERATOR, LESION, RADIOFREQUENCY
- Charges
- 118