FDA Import Refusal 231-0781160-0/1/1 — CareFusion DR 203 LTD
The FDA refused shipment 231-0781160-0/1/1 from CareFusion DR 203 LTD (Dominican Republic) on July 26, 2011. The refused product falls under Devices — INSTRUMENT, BIOPSY. Cited charge: 508 This firm has 3 other import refusals on record.
Refusal Details
- Date
- July 26, 2011
- Country
- Dominican Republic
- Product Category
- Devices
- Product Code
- 78KNW INSTRUMENT, BIOPSY
- Charges
- 508