FDA Warning Letter — The Lebanon Corporation, Inc.

Case 286458 — FEI 1824818

The FDA took a Warning Letter action against The Lebanon Corporation, Inc. on May 17, 2012 (Lebanon, IN). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
The Lebanon Corporation, Inc.
Date
May 17, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Lebanon, IN (United States)