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FDA Warning Letter — R82 A/S

Case 412111 — FEI 3001657382

The FDA took a Warning Letter action against R82 A/S on Oct 18, 2013 (Gedved, Denmark). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
R82 A/S
Date
Oct 18, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Gedved (Denmark)

Facility

Recent inspections

Other compliance actions

FDA data resources

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