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KEDPLASMA LLC 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 2077886.

KEDPLASMA LLC

Flagstaff, Arizona, United States
Issue DateAugust 30, 2018
FEI Number2077886
CountryUnited States
Status
No Warning Letter
Product Type
Biologics
KEDPLASMA LLC FDA Form 483, Flagstaff, Arizona, August 30, 2018