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FDA Inspection
•Cody Laboratories, Inc.•July 24, 2009

Cody Laboratories, Inc. – FDA Inspection, Jul 24, 2009

Record Details

This FDA Inspection record concerns Cody Laboratories, Inc., with an inspection on July 24, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Cody Laboratories, Inc.
Inspection Date
July 24, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 5a06dce8-a932-40c5-9514-ab0124d7485e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
612683
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

2
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.180(e)(1)Review of representative number of batches

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cody Laboratories, Inc.

5
DateClassificationOfficeProject area
December 8, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 30, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 12, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 18, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 27, 2010VAICenter for Drug Evaluation and ResearchUnapproved and Misbranded Drugs
Other documents for Cody Laboratories, Inc.
  • FDA Inspection 1034453 - 2017-12-08
  • FDA Inspection 902313 - 2014-10-30
  • FDA Inspection 805118 - 2012-10-12
  • FDA Inspection 712399 - 2011-02-18
  • FDA Inspection 682313 - 2010-08-27

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