FDA Import Refusal AEK-9001522-9/1/1 — Formaggia Srl
The FDA refused shipment AEK-9001522-9/1/1 from Formaggia Srl (Italy) on Aug 28, 2007. The refused product falls under Devices — ELECTRODE, CUTANEOUS. Cited charge: 84 This firm has 2 other import refusals on record.
Refusal details
- Date
- Aug 28, 2007
- Country
- Italy
- Product Category
- Devices
- Product Code
- 84GXY ELECTRODE, CUTANEOUS
- Charges
- 84