# Hydrofera, LLC – FDA Inspection, Aug 23, 2017

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

> FDA inspection 1025048 of Hydrofera, LLC, August 23, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 846921 - 2013-09-04
- [FDA Inspection 735431 - 2011-07-20](https://www.keypedia.com/records/fda_inspections/hydrofera-llc/b4d081d9-ea42-47a7-8b3f-fdf2af19b728)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

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