FDA Import Refusal 336-3022855-4/12/1 — KLS Martin GmbH & Co. KG
The FDA refused shipment 336-3022855-4/12/1 from KLS Martin GmbH & Co. KG (Germany) on Aug 3, 2018. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 126,508 This firm has 2 other import refusals on record.
Refusal details
- Date
- Aug 3, 2018
- Country
- Germany
- Product Category
- Devices
- Product Code
- 79GEX POWERED LASER SURGICAL INSTRUMENTS
- Charges
- 126,508