FDA Import Refusal 799-8490279-8/11/1A — Philips North America LLC
The FDA refused shipment 799-8490279-8/11/1A from Philips North America LLC (United States) on February 1, 2019. The refused product falls under Devices — AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE). Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- February 1, 2019
- Country
- United States
- Product Category
- Devices
- Product Code
- 74MKJ AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE)
- Charges
- 118