FDA Import Refusal 112-9003264-1/1/1 — Fielmann Group AG
The FDA refused shipment 112-9003264-1/1/1 from Fielmann Group AG (Germany) on Nov 5, 2010. The refused product falls under Devices — LENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT. Cited charge: 118 This firm has 2 other import refusals on record.
Refusal details
- Date
- Nov 5, 2010
- Country
- Germany
- Product Category
- Devices
- Product Code
- 86NJH LENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT
- Charges
- 118