# FDA Inspection 970549 - Diazyme Laboratories - April 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/diazyme-laboratories/b65bcbda-5b93-4269-8d13-a2d55d047149
Source feed: FDA_Inspections

> FDA Inspection 970549 for Diazyme Laboratories on April 20, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 970549
- Company Name: Diazyme Laboratories
- Inspection Date: 2016-04-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 741128 - 2011-08-25](https://www.keypedia.com/records/fda_inspections/diazyme-laboratories/12d57ddf-5ccc-44db-a155-651ace6d4e48)

Company: https://www.keypedia.com/companies/diazyme-laboratories/bab32d66-37af-42a8-b6cb-bc1a152afaf3

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7