FDA Import Refusal MH9-2071187-5/11/16 — ASTROLABE FABRICACAO DE IMPLANTES

ASTROLABE FABRICACAO DE IMPLANTES — FEI 3013677270

The FDA refused shipment MH9-2071187-5/11/16 from ASTROLABE FABRICACAO DE IMPLANTES (Portugal) on Aug 15, 2017. The refused product falls under Devices — GUIDE, SURGICAL, INSTRUMENT. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 15, 2017
Country
Portugal
Product Category
Devices
Product Code
79FZX GUIDE, SURGICAL, INSTRUMENT
Charges
118,3280,341

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