FDA Import Refusal AEK-1135606-6/1/1 — Philips North America, LLC
The FDA refused shipment AEK-1135606-6/1/1 from Philips North America, LLC (United States) on Aug 8, 2013. The refused product falls under Devices — GENERATOR, OXYGEN, PORTABLE. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 8, 2013
- Country
- United States
- Product Category
- Devices
- Product Code
- 73CAW GENERATOR, OXYGEN, PORTABLE
- Charges
- 341