FDA Import Refusal AEK-7558180-7/1/1 — MORIA S.A.
The FDA refused shipment AEK-7558180-7/1/1 from MORIA S.A. (France) on Oct 5, 2005. The refused product falls under Devices — KERATOME, AC-POWERED. Cited charge: 341 This firm has 1 other import refusal on record.
Refusal details
- Date
- Oct 5, 2005
- Country
- France
- Product Category
- Devices
- Product Code
- 86HNO KERATOME, AC-POWERED
- Charges
- 341