Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1831750.
Observations7
Issue DateJuly 11, 2015
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections5
Establishment Details
Firm
Stryker Medical Division of Stryker Corporation
Location
Portage, Michigan, United States
FEI Number
1831750
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
July 11, 2015
Country
United States
Inspection History, 2009 to 2024
VAI4
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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