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 3002807145.
Observations1
Issue DateFebruary 24, 2023
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Pausch Medical GmbH
Location
Erlangen, -, Germany
FEI Number
3002807145
Product Type
Devices
Issue Date
February 24, 2023
Country
Germany
Inspection History, 2018 to 2026
NAI2
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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