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FDA Inspection
•Medical Instrument Development Laboratories, Inc.•October 9, 2026

Medical Instrument Development Laboratories, Inc. – FDA Inspection, Oct 9, 2026

Record Details

This FDA Inspection record concerns Medical Instrument Development Laboratories, Inc., with an inspection on October 9, 2026, issued by the Center for Devices and Radiological Health, covering devices.

Company
Medical Instrument Development Laboratories, Inc.
Inspection Date
October 9, 2026
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 9829cc69-0388-4a34-89ba-5c538e7bd778

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1340346
Project area
Compliance: Devices

FDA Citations

1
  1. ISO 13485:2016 Clause 8.5.2Corrective actions not proportionate to the effects of nonconformities

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Medical Instrument Development Laboratories, Inc.

5
DateClassificationOfficeProject area
August 13, 2025NAISan Francisco District OfficePostmarket Assurance: Medical Devices
August 28, 2024Not classifiedSan Francisco District Office
August 14, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
March 14, 2013NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 1, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Medical Instrument Development Laboratories, Inc.
  • FDA Inspection 1279924 - 2025-08-13
  • FDA Inspection 1250119 - 2024-08-28
  • FDA Inspection 937087 - 2015-08-14
  • FDA Inspection 823014 - 2013-03-14
  • FDA Inspection 655821 - 2010-04-01

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