# Hydrofera, LLC – FDA Inspection, Jul 20, 2011

Source: https://www.keypedia.com/records/fda_inspections/hydrofera-llc/b4d081d9-ea42-47a7-8b3f-fdf2af19b728
Source feed: FDA_Inspections

> FDA inspection 735431 of Hydrofera, LLC, July 20, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 735431
- Company Name: Hydrofera, LLC
- Inspection Date: 2011-07-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1025048 - 2017-08-23](https://www.keypedia.com/records/fda_inspections/hydrofera-llc/0789e502-72c9-46c8-a6cd-7a53044b8285)
- FDA Inspection 846921 - 2013-09-04

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