Cytovance Biologics, Inc.

Form 483FOIA Uncovered

Oklahoma City, OklahomaFEI 3006341547Issued May 09, 2019

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3006341547.

ObservationsNot available

Issue DateMay 09, 2019

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Cytovance Biologics, Inc.
Location: Oklahoma City, Oklahoma
FEI Number: 3006341547
Product Type: Drugs
Issue Date: May 09, 2019
Country: United States

Inspection History, 2017 to 2026

NAI1

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Cytovance Biologics, Inc. FDA Form 483, Oklahoma City, Oklahoma, May 9, 2019