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Teleflex Medical 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 3004943382.

Teleflex Medical

Durham, North Carolina, United States
Issue DateMarch 23, 2010
FEI Number3004943382
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Teleflex Medical FDA Form 483, Durham, North Carolina, March 23, 2010