FDA Import Refusal AEK-8835219-6/1/1 — BEIJING GLOBALIPL DEVELOPMENT CO Ltd

BEIJING GLOBALIPL DEVELOPMENT CO Ltd — FEI 3012799115

The FDA refused shipment AEK-8835219-6/1/1 from BEIJING GLOBALIPL DEVELOPMENT CO Ltd (China) on Aug 31, 2011. The refused product falls under Devices — DIATHERMY, SHORTWAVE, FOR USE OTHER THAN APPLYING THERAPEUTIC DEEP HEAT. Cited charges: 118,237,84 This firm has 4 other import refusals on record.

Refusal details

Date
Aug 31, 2011
Country
China
Product Category
Devices
Product Code
89ILX DIATHERMY, SHORTWAVE, FOR USE OTHER THAN APPLYING THERAPEUTIC DEEP HEAT
Charges
118,237,84

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