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FDA Inspection
•Allos Therapeutics, Inc.•August 18, 2009

Allos Therapeutics, Inc. – FDA Inspection, Aug 18, 2009

Record Details

This FDA Inspection record concerns Allos Therapeutics, Inc., with an inspection on August 18, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Allos Therapeutics, Inc.
Inspection Date
August 18, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 1058648f-a838-47f2-a70a-ba82a5ee7f33

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
614637
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

4
  1. 21 CFR 312.50General responsibilities of sponsors
  2. 21 CFR 312.59Records of unused drug disposition
  3. 21 CFR 312.53(c)(1)Investigator statement (FDA 1572)
  4. 21 CFR 312.52(a)Transfer of obligations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Allos Therapeutics, Inc.

1
DateClassificationOfficeProject area
July 21, 2011NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
Other documents for Allos Therapeutics, Inc.
  • FDA Inspection 741032 - 2011-07-21

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