# FDA Inspection 1092412 - HydroCision, Inc. - June 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/hydrocision-inc/875c5fcb-ddac-48e0-9ade-1dc4c85d56a3
Source feed: FDA_Inspections

> FDA Inspection 1092412 for HydroCision, Inc. on June 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092412
- Company Name: HydroCision, Inc.
- Inspection Date: 2019-06-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1092412 - 2019-06-07](https://www.keypedia.com/records/fda_inspections/hydrocision-inc/13da3c86-2a77-42c6-8b67-9f04957bf67b)
- [FDA Inspection 871352 - 2014-04-16](https://www.keypedia.com/records/fda_inspections/hydrocision-inc/3a3c18b2-7661-4c36-8435-c146891bdec5)
- [FDA Inspection 771019 - 2012-03-07](https://www.keypedia.com/records/fda_inspections/hydrocision-inc/1a3cfa7d-64b3-4557-8b54-0c89f037fc24)
- [FDA Inspection 586534 - 2009-05-08](https://www.keypedia.com/records/fda_inspections/hydrocision-inc/83b36ef3-5840-44af-8d82-4f6cd8918a74)

Company: https://www.keypedia.com/companies/hydrocision-inc/192c718e-48fb-4415-8315-96957041029b

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