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Mid America Clinical Laboratories St. Vincent Women's Hosp. 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.

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Mid America Clinical Laboratories St. Vincent Women's Hosp.

Indianapolis, Indiana, United States
Issue DateNovember 28, 2016
FEI Number3011268785
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
Mid America Clinical Laboratories St. Vincent Women's Hosp. FDA Form 483, Indianapolis, Indiana, November 28, 2016