FDA Import Refusal AEK-1040811-7/1/1 — Misonix, Inc.
The FDA refused shipment AEK-1040811-7/1/1 from Misonix, Inc. (United States) on July 27, 2015. The refused product falls under Devices — INSTRUMENT, ULTRASONIC SURGICAL. Cited charge: 341
Refusal Details
- Date
- July 27, 2015
- Country
- United States
- Product Category
- Devices
- Product Code
- 79LFL INSTRUMENT, ULTRASONIC SURGICAL
- Charges
- 341