FDA Import Refusal 101-5697876-9/41/1 — Lap GmbH Laser Applikationen
The FDA refused shipment 101-5697876-9/41/1 from Lap GmbH Laser Applikationen (Germany) on Dec 6, 2017. The refused product falls under Devices — MONITOR, PATIENT POSITION, LIGHT-BEAM. Cited charge: 47 This firm has 3 other import refusals on record.
Refusal details
- Date
- Dec 6, 2017
- Country
- Germany
- Product Category
- Devices
- Product Code
- 90IWE MONITOR, PATIENT POSITION, LIGHT-BEAM
- Charges
- 47