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STERIMED, Inc. 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 1053306.

STERIMED, Inc.

ridgeville, South Carolina, United States
Issue DateDecember 14, 2016
FEI Number1053306
CountryUnited States
Status
No Warning Letter
Product Type
Devices
STERIMED, Inc. FDA Form 483, ridgeville, South Carolina, December 14, 2016