FDA Import Refusal K51-0065292-1/1/1 — Biomet, Inc.
The FDA refused shipment K51-0065292-1/1/1 from Biomet, Inc. (United States) on October 14, 2008. The refused product falls under Devices — APPLIANCE, NAIL/BLADE/PLATE COMBINATION, SINGLE COMPONENT. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- October 14, 2008
- Country
- United States
- Product Category
- Devices
- Product Code
- 87KWK APPLIANCE, NAIL/BLADE/PLATE COMBINATION, SINGLE COMPONENT
- Charges
- 341