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Octapharma Plasma 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.

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Octapharma Plasma Inc

Omaha, Nebraska, United States
Issue DateJune 07, 2011
FEI Number3006604254
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
Octapharma Plasma Inc FDA Form 483, Omaha, Nebraska, June 7, 2011