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FDA Inspection
•Ben Venue Laboratories Inc•May 13, 2009

Ben Venue Laboratories Inc – FDA Inspection, May 13, 2009

Record Details

This FDA Inspection record concerns Ben Venue Laboratories Inc, with an inspection on May 13, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Ben Venue Laboratories Inc
Inspection Date
May 13, 2009
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · e41eda5f-0c17-4eb1-959a-8d6e092e8f28

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
588705
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.110(a)Control procedures to monitor and validate performance
  2. 21 CFR 211.100(a)Absence of Written Procedures
  3. 21 CFR 211.192Investigations of discrepancies, failures
  4. 21 CFR 211.192Written record of investigation incomplete

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Ben Venue Laboratories Inc

9
DateClassificationOfficeProject area
June 6, 2014OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 29, 2013OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 2, 2011OAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 25, 2011OAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
March 11, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Ben Venue Laboratories Inc
  • FDA Inspection 882591 - 2014-06-06
  • FDA Inspection 826465 - 2013-03-29
  • FDA Inspection 759506 - 2011-12-02
  • FDA Inspection 729039 - 2011-05-25
  • FDA Inspection 714969 - 2011-03-11

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