FDA Import Refusal 799-9342434-7/11/2 — Johnson & Johnson K.K.

Johnson & Johnson K.K. — FEI 3004862850

The FDA refused shipment 799-9342434-7/11/2 from Johnson & Johnson K.K. (Japan) on Dec 17, 2018. The refused product falls under Devices — LAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED. Cited charge: 118 This firm has 3 other import refusals on record.

Refusal details

Date
Dec 17, 2018
Country
Japan
Product Category
Devices
Product Code
78NLM LAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED
Charges
118

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