FDA Import Refusal SCS-6412362-4/11/1A — BIOMAK SP.J.

BIOMAK SP.J. — FEI 3013975737

The FDA refused shipment SCS-6412362-4/11/1A from BIOMAK SP.J. (Poland) on Aug 27, 2019. The refused product falls under Devices — EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE. Cited charges: 118,3280

Refusal details

Date
Aug 27, 2019
Country
Poland
Product Category
Devices
Product Code
79KCW EPILATOR, HIGH FREQUENCY, NEEDLE-TYPE
Charges
118,3280

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.