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FDA Inspection
•Bell-More Labs, Inc.•March 17, 2009

Bell-More Labs, Inc. – FDA Inspection, Mar 17, 2009

Record Details

This FDA Inspection record concerns Bell-More Labs, Inc., with an inspection on March 17, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Bell-More Labs, Inc.
Inspection Date
March 17, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b03e68a4-eba9-4082-981a-b621576dead8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
569622
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
  2. 21 CFR 211.68(a)Calibration/Inspection/Checking not done

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Bell-More Labs, Inc.

7
DateClassificationOfficeProject area
April 3, 2024Not classifiedBaltimore District OfficeDrug Quality Assurance
June 7, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 26, 2018OAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 26, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 13, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Bell-More Labs, Inc.
  • FDA Inspection 1234928 - 2024-04-03
  • FDA Inspection 1143441 - 2021-06-07
  • FDA Inspection 1066757 - 2018-09-26
  • FDA Inspection 979342 - 2016-05-26
  • FDA Inspection 918971 - 2015-03-13

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