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Gelflex Laboratories 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 1000426389.

Gelflex Laboratories

Malaga, -, Australia
Issue DateJanuary 30, 2015
FEI Number1000426389
CountryAustralia
Status
No Warning Letter
Product Type
Devices
Gelflex Laboratories FDA Form 483, Malaga, January 30, 2015