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Randox Laboratories, Limited 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 3004493545.

Randox Laboratories, Limited

Crumlin, -, United Kingdom
Issue DateNovember 29, 2012
FEI Number3004493545
CountryUnited Kingdom
Status
No Warning Letter
Product Type
Devices
Randox Laboratories, Limited FDA Form 483, Crumlin, November 29, 2012