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FDA Inspection
•Synexus Clinical Research US, Inc.•May 11, 2017

Synexus Clinical Research US, Inc. – FDA Inspection, May 11, 2017

Record Details

This FDA Inspection record concerns Synexus Clinical Research US, Inc., with an inspection on May 11, 2017, issued by the Dallas District Office, covering human drugs.

Company
Synexus Clinical Research US, Inc.
Inspection Date
May 11, 2017
Product Type
Human Drugs
Office
Dallas District Office
Person
  • Camille D. Brown (Company Rep)
View Company Profile

ID · 8e120362-1646-427b-b6d4-19ce12823d60

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1015462
FDA center
Human Drugs
Project area
Bioresearch Monitoring
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 312.60FD-1572, protocol compliance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Synexus Clinical Research US, Inc.

1
DateClassificationOfficeProject area
August 4, 2017Not classifiedDallas District Office
Other documents for Synexus Clinical Research US, Inc.
  • FDA Inspection 1029957 - 2017-08-04

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