FDA Import Refusal 002-4232059-6/11/1 — BIOMAK MALGORZATA
The FDA refused shipment 002-4232059-6/11/1 from BIOMAK MALGORZATA (Poland) on Sep 25, 2017. The refused product falls under Devices — EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE. Cited charges: 118,16,3280,333
Refusal details
- Date
- Sep 25, 2017
- Country
- Poland
- Product Category
- Devices
- Product Code
- 79KCW EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE
- Charges
- 118,16,3280,333