Stryker Corporation

Form 483

San Jose, California, United StatesFEI 2936485Issued September 18, 2015

View FDA's Record for This Firm

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 2936485.

Observations2

Issue DateSeptember 18, 2015

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Stryker Corporation
Location: San Jose, California, United States
FEI Number: 2936485
Product Type: Devices
Issue Date: September 18, 2015
Country: United States

Inspection History, 2009 to 2019

NAI1

VAI6

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Stryker Corporation FDA Form 483, San Jose, California, September 18, 2015