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Aspire Houston Fertility Institute 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 1000543561.

Aspire Houston Fertility Institute

Houston, Texas, United States
Issue DateNovember 01, 2010
FEI Number1000543561
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
Aspire Houston Fertility Institute FDA Form 483, Houston, Texas, November 1, 2010