Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3002808267.
Observations3
Issue DateApril 28, 2022
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
LivaNova Deutschland GmbH
Location
Munich, -, Germany
FEI Number
3002808267
Product Type
Devices
Issue Date
April 28, 2022
Country
Germany
Inspection History, 2011 to 2022
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
Talk to a Specialist