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 3003366417.
Observations3
Issue DateJuly 26, 2018
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
LRE Medical GmbH
Location
Nordlingen, -, Germany
FEI Number
3003366417
Product Type
Devices
Issue Date
July 26, 2018
Country
Germany
Inspection History, 2017 to 2018
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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