FDA Import Refusal 334-2783270-5/61/1 — KEYSIGHT TECHNOLOGIES

KEYSIGHT TECHNOLOGIES — FEI 3013665423

The FDA refused shipment 334-2783270-5/61/1 from KEYSIGHT TECHNOLOGIES (Belgium) on Aug 17, 2017. The refused product falls under Radiological Health — LASER AIMING PRODUCT, VISIBLE, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS. Cited charge: 47

Refusal details

Date
Aug 17, 2017
Country
Belgium
Product Category
Radiological Health
Product Code
95REU LASER AIMING PRODUCT, VISIBLE, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
Charges
47

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