FDA Import Refusal 799-3413677-9/11/1 — bioLytical Laboratories, Inc.

bioLytical Laboratories, Inc. — FEI 3003871407

The FDA refused shipment 799-3413677-9/11/1 from bioLytical Laboratories, Inc. (Canada) on Oct 3, 2019. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 3, 2019
Country
Canada
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118

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