FDA Import Refusal 799-5392265-2/11/4 — Artron Laboratories, Inc.

Artron Laboratories, Inc. — FEI 3005445066

The FDA refused shipment 799-5392265-2/11/4 from Artron Laboratories, Inc. (Canada) on May 10, 2018. The refused product falls under Devices — KIT, TEST, MULTIPLE DRUGS OF ABUSE, OVER THE COUNTER. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
May 10, 2018
Country
Canada
Product Category
Devices
Product Code
91MVO KIT, TEST, MULTIPLE DRUGS OF ABUSE, OVER THE COUNTER
Charges
118,508

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