FDA Import Refusal 110-0708862-8/1/1 — Bayer Corp
The FDA refused shipment 110-0708862-8/1/1 from Bayer Corp (United States) on Aug 13, 2004. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 13, 2004
- Country
- United States
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118