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Deaconess Center For Reproductive Health 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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Deaconess Center For Reproductive Health

Oklahoma City, Oklahoma, United States
Issue DateAugust 03, 2011
FEI Number3008805514
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
Deaconess Center For Reproductive Health FDA Form 483, Oklahoma City, Oklahoma, August 3, 2011