FDA Warning Letter — ARKRAY, Inc.

Case 446446 — FEI 3002807423

The FDA took a Warning Letter action against ARKRAY, Inc. on April 10, 2015 (Kyoto, Japan). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
ARKRAY, Inc.
Date
April 10, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Kyoto (Japan)