FDA Import Refusal AEK-0537322-7/1/1 — Philips Oy
The FDA refused shipment AEK-0537322-7/1/1 from Philips Oy (Finland) on Dec 24, 2014. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charge: 341 This firm has 3 other import refusals on record.
Refusal details
- Date
- Dec 24, 2014
- Country
- Finland
- Product Category
- Devices
- Product Code
- 73CAF NEBULIZER (DIRECT PATIENT INTERFACE)
- Charges
- 341