# FDA Inspection 1018178 - Fisher Diagnostics - May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/fisher-diagnostics/59bce508-9ac7-4e99-8f65-3c9759d3105d
Source feed: FDA_Inspections

> FDA Inspection 1018178 for Fisher Diagnostics on May 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018178
- Company Name: Fisher Diagnostics
- Inspection Date: 2017-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.keypedia.com/companies/fisher-diagnostics/25f1746f-740f-45f0-a724-e01f8d973870

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