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FDA Inspection
•Bell Pharmaceuticals, Inc•April 5, 2013

Bell Pharmaceuticals, Inc – FDA Inspection, Apr 5, 2013

Record Details

This FDA Inspection record concerns Bell Pharmaceuticals, Inc, with an inspection on April 5, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Bell Pharmaceuticals, Inc
Inspection Date
April 5, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 9d791269-7da1-43fc-8b4d-f6c365418ff2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
826998
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.122(d)Label storage access limited to authorized personnel
  2. 21 CFR 211.188Prepared for each batch, include complete information
  3. Failure of responsible person to report AE (non-RX Drug)

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Bell Pharmaceuticals, Inc

5
DateClassificationOfficeProject area
June 18, 2025VAIMinneapolis District OfficeDrug Quality Assurance
April 6, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 20, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 12, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 15, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Bell Pharmaceuticals, Inc
  • FDA Inspection 1271571 - 2025-06-18
  • FDA Inspection 1047160 - 2018-04-06
  • FDA Inspection 955992 - 2015-11-20
  • FDA Inspection 697960 - 2010-11-12
  • FDA Inspection 582576 - 2009-05-15

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