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 3002808493.
Observations1
Issue DateJuly 21, 2011
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Willy Rusch GmbH a div of Teleflex Medical
Location
Kernen Im Remstal, -, Germany
FEI Number
3002808493
Product Type
Devices
Issue Date
July 21, 2011
Country
Germany
Inspection History, 2011 to 2014
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.