FDA Import Refusal AEK-6073593-0/11/1 — CENTRALE FILLERS
The FDA refused shipment AEK-6073593-0/11/1 from CENTRALE FILLERS (France) on Jul 11, 2019. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charges: 118,237,3280 This firm has 3 other import refusals on record.
Refusal details
- Date
- Jul 11, 2019
- Country
- France
- Product Category
- Devices
- Product Code
- 87MOZ ACID, HYALURONIC, INTRAARTICULAR
- Charges
- 118,237,3280