# Hardy Diagnostics – FDA Inspection, Jun 9, 2023

Source: https://www.keypedia.com/records/fda_inspections/hardy-diagnostics/c6c0eff8-6f0a-49eb-b8a2-230bb6eff13f
Source feed: FDA_Inspections

> FDA inspection 1207738 of Hardy Diagnostics, June 09, 2023. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1207738
- Company Name: Hardy Diagnostics
- Inspection Date: 2023-06-09
- 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: 3

## Related Documents

- FDA Inspection 1074037 - 2018-11-28
- FDA Inspection 947527 - 2015-11-05
- FDA Inspection 723955 - 2011-04-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/marlo-ian-m-alintanahin/a37da927-b369-4753-b275-41743556f25e)

Company: https://www.keypedia.com/companies/hardy-diagnostics/c29846c3-0f97-4891-8e74-6e80165a3355

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