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Covidien Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed 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 this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3001236355.

Covidien

San Jose, California, United States
Issue DateApril 04, 2012
FEI Number3001236355
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Covidien FDA Form 483, San Jose, California, April 4, 2012