FDA Import Refusal AEK-6405721-5/1/1 — OmniLife Science
The FDA refused shipment AEK-6405721-5/1/1 from OmniLife Science (United States) on August 20, 2004. The refused product falls under Devices — INSTRUMENT, STEREOTAXIC. Cited charge: 118 This firm has 2 other import refusals on record.
Refusal Details
- Date
- August 20, 2004
- Country
- United States
- Product Category
- Devices
- Product Code
- 84HAW INSTRUMENT, STEREOTAXIC
- Charges
- 118