FDA Import Refusal M76-1830736-9/1/1 — Pierenkemper Gmbh

Pierenkemper Gmbh — FEI 3005923596

The FDA refused shipment M76-1830736-9/1/1 from Pierenkemper Gmbh (Germany) on Sep 6, 2012. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Sep 6, 2012
Country
Germany
Product Category
Devices
Product Code
80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
Charges
118,508

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