Atlas

FDA-Inspected Site

Cytovance Biologics, Inc.

3 FDA inspections are on record for Cytovance Biologics, Inc. in Oklahoma City, United States.

483· Form 483 issued

Oklahoma City, United States · Last updated July 9, 2026

Overview

  • 3 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2019-05-09.

At a glance

Inspections

3

Form 483s

2

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
1 May 2019 – 9 May 2019Human Drugs483On file
23 Apr 2018 – 27 Apr 2018BiologicsClean
11 Jul 2017 – 20 Jul 2017Human Drugs483On file

Investigators

FDA investigators tied to this site in the record.

Margaret M Annes2 insp.
Teresita C Mercado1 insp.
Meihong Liu1 insp.
Priscilla M Pastrana1 insp.
Hector A Carrero1 insp.
Darcel T Bigelow1 insp.

Full site report

Get the verbatim findings behind Cytovance Biologics, Inc.'s 2 Form 483s

The full inspection record, as Atlas holds it, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat