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FDA Inspection
•B&B Medical Technologies, Inc.•April 17, 2025

B&B Medical Technologies, Inc. – FDA Inspection, Apr 17, 2025

Record Details

This FDA Inspection record concerns B&B Medical Technologies, Inc., with an inspection on April 17, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company
B&B Medical Technologies, Inc.
Inspection Date
April 17, 2025
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Daniel J. Lahar (FDA Associated Person)
View Company Profile

ID · 97a803fc-72c7-42fd-8eec-b9b15c99668c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1267852
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 820.25(b)Training records
  2. 21 CFR 820.22Quality Audit/Reaudit - conducted
  3. 21 CFR 820.20(c)Management review dates

Full citation text and observation details available on the Dashboard.

Other FDA inspections of B&B Medical Technologies, Inc.

3
DateClassificationOfficeProject area
February 5, 2026NAILos Angeles District OfficePostmarket Assurance: Medical Devices
June 13, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 3, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for B&B Medical Technologies, Inc.
  • FDA Inspection 1301456 - 2026-02-05
  • FDA Inspection 883600 - 2014-06-13
  • FDA Inspection 796466 - 2012-08-03

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