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FDA Inspection
•Anderson & Collins Clinical Research Inc.•March 20, 2017

Anderson & Collins Clinical Research Inc. – FDA Inspection, Mar 20, 2017

Record Details

This FDA Inspection record concerns Anderson & Collins Clinical Research Inc., with an inspection on March 20, 2017, issued by the New Jersey District Office, covering human drugs.

Company
Anderson & Collins Clinical Research Inc.
Inspection Date
March 20, 2017
Product Type
Human Drugs
Office
New Jersey District Office
People
  • Anastasia I. Onuorah (Company Rep)
  • Nina Yang (Company Rep)
View Company Profile

ID · c9e7a126-a8e9-4a08-8afd-809676b5c632

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1008182
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 Anderson & Collins Clinical Research Inc.

2
DateClassificationOfficeProject area
July 25, 2012NAICenter for Biologics Evaluation and ResearchBioresearch Monitoring
October 21, 2008NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Anderson & Collins Clinical Research Inc.
  • FDA Inspection 791930 - 2012-07-25
  • FDA Inspection 543402 - 2008-10-21

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