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FDA Inspection
•Diazyme Laboratories•August 25, 2011

Diazyme Laboratories – FDA Inspection, Aug 25, 2011

Record Details

This FDA Inspection record concerns Diazyme Laboratories, with an inspection on August 25, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Diazyme Laboratories
Inspection Date
August 25, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 12d57ddf-5ccc-44db-a155-651ace6d4e48

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
741128
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 806.20(b)(4)Justification for not reporting

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Diazyme Laboratories

1
DateClassificationOfficeProject area
April 20, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Diazyme Laboratories
  • FDA Inspection 970549 - 2016-04-20

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