FDA Import Refusal 799-0693728-3/1/1 — Philips North America LLC
The FDA refused shipment 799-0693728-3/1/1 from Philips North America LLC (United States) on October 25, 2013. The refused product falls under Devices — OVER-THE-COUNTER AUTOMATED EXTERNAL DEFIBRILLATOR. Cited charges: 118,508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- October 25, 2013
- Country
- United States
- Product Category
- Devices
- Product Code
- 74NSA OVER-THE-COUNTER AUTOMATED EXTERNAL DEFIBRILLATOR
- Charges
- 118,508