FDA Import Refusal 8DS-0313151-5/11/1 — Fisher & Paykel Healthcare, Ltd.
The FDA refused shipment 8DS-0313151-5/11/1 from Fisher & Paykel Healthcare, Ltd. (New Zealand) on May 16, 2017. The refused product falls under Devices — HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE). Cited charges: 118,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- May 16, 2017
- Country
- New Zealand
- Product Category
- Devices
- Product Code
- 73BTT HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)
- Charges
- 118,508