FDA Warning Letter — Medibo N.V.

Case 69823 — FEI 3004468271

The FDA took a Warning Letter action against Medibo N.V. on Oct 2, 2009 (Hamont-Achel, Belgium). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Medibo N.V.
Date
Oct 2, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Hamont-Achel (Belgium)

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