FDA Import Refusal D99-1433456-9/11/1B — Angiplast Private Limited
The FDA refused shipment D99-1433456-9/11/1B from Angiplast Private Limited (India) on July 3, 2019. The refused product falls under Devices — SET, I.V. FLUID TRANSER. Cited charges: 2780,78 This firm has 4 other import refusals on record.
Refusal Details
- Date
- July 3, 2019
- Country
- India
- Product Category
- Devices
- Product Code
- 80LHI SET, I.V. FLUID TRANSER
- Charges
- 2780,78