# HQ, Inc. – FDA Inspection, Sep 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/hq-inc/efd0fb6c-6aea-408c-97f6-e879cd2ec6dd
Source feed: FDA_Inspections

> FDA inspection 1026395 of HQ, Inc., September 22, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026395
- Company Name: HQ, Inc.
- Inspection Date: 2017-09-22
- 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: 8

## Related Documents

- [FDA Inspection 1101181 - 2019-08-30](https://www.keypedia.com/records/fda_inspections/hq-inc/dc912893-aa50-4e81-a63e-1dad3948ca34)
- [FDA Inspection 793451 - 2012-08-03](https://www.keypedia.com/records/fda_inspections/hq-inc/ddd14929-fcf1-4c00-832c-7b38487cd537)

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/hq-inc/b1e49406-fce9-4241-8b5c-baa3397f7387

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