# HQ, Inc. – FDA Inspection, Aug 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/hq-inc/dc912893-aa50-4e81-a63e-1dad3948ca34
Source feed: FDA_Inspections

> FDA inspection 1101181 of HQ, Inc., August 30, 2019. Classification: No Action Indicated (NAI). 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: 1101181
- Company Name: HQ, Inc.
- Inspection Date: 2019-08-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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 1026395 - 2017-09-22](https://www.keypedia.com/records/fda_inspections/hq-inc/efd0fb6c-6aea-408c-97f6-e879cd2ec6dd)
- [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