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 3009829742.
Observations3
Issue DateSeptember 26, 2019
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Neuromedex GmbH
Location
Hamburg, -, Germany
FEI Number
3009829742
Product Type
Devices
Issue Date
September 26, 2019
Country
Germany
Inspection History, 2019 to 2026
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.