FDA Warning Letter — LISA Laser Products OHG

Case 394724 — FEI 3003168101

The FDA took a Warning Letter action against LISA Laser Products OHG on May 8, 2013 (Katlenburg-Lindau, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
LISA Laser Products OHG
Date
May 8, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Katlenburg-Lindau (Germany)

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