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FDA Import Refusal AN1-0251313-0/11/1 — LaserOptek

LaserOptek — FEI 3007181527

The FDA refused shipment AN1-0251313-0/11/1 from LaserOptek (South Korea) on Jan 6, 2021. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charge: 341 This firm has 1 other import refusal on record.

Refusal details

Date
Jan 6, 2021
Country
South Korea
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
341

Other import refusals

FDA data resources

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