FDA Import Refusal 224-0360975-7/1/24 — Covidien LP
The FDA refused shipment 224-0360975-7/1/24 from Covidien LP (United States) on August 4, 2008. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- August 4, 2008
- Country
- United States
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 118