# FDA Inspection 1025048 - Hydrofera, LLC - August 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/hydrofera-llc/0789e502-72c9-46c8-a6cd-7a53044b8285
Source feed: FDA_Inspections

> FDA Inspection 1025048 for Hydrofera, LLC on August 23, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025048
- Company Name: Hydrofera, LLC
- Inspection Date: 2017-08-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025048 - 2017-08-23](https://www.keypedia.com/records/fda_inspections/hydrofera-llc/02603b43-c064-4841-81c5-24b4aaf7cb7d)
- [FDA Inspection 846921 - 2013-09-04](https://www.keypedia.com/records/fda_inspections/hydrofera-llc/1c93819d-3315-4d10-b7be-5a8a2ff2fe84)
- [FDA Inspection 735431 - 2011-07-20](https://www.keypedia.com/records/fda_inspections/hydrofera-llc/b4d081d9-ea42-47a7-8b3f-fdf2af19b728)

Company: https://www.keypedia.com/companies/hydrofera-llc/c4f73cb6-73ab-4aab-9fe2-914aff435aa2

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