FDA Import Refusal AEK-0171846-5/1/1 — Biotekne Srl
The FDA refused shipment AEK-0171846-5/1/1 from Biotekne Srl (Italy) on May 31, 2012. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,341,508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- May 31, 2012
- Country
- Italy
- Product Category
- Devices
- Product Code
- 80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
- Charges
- 118,341,508