FDA Import Refusal AEK-5324892-5/12/1 — THE MANUFACTURER IS SHANDONG BOU
The FDA refused shipment AEK-5324892-5/12/1 from THE MANUFACTURER IS SHANDONG BOU (China) on Dec 4, 2018. The refused product falls under Devices — ACID, HYALURONIC, INTRAARTICULAR. Cited charges: 118,237,3280,333,84
Refusal details
- Date
- Dec 4, 2018
- Country
- China
- Product Category
- Devices
- Product Code
- 87MOZ ACID, HYALURONIC, INTRAARTICULAR
- Charges
- 118,237,3280,333,84