# Product Quest Manufacturing LLC – FDA Inspection, Jan 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/product-quest-manufacturing-llc/f319cb49-16a3-4fa3-9e5b-fd0f8b88e230
Source feed: FDA_Inspections

> FDA inspection 1000036 of Product Quest Manufacturing LLC, January 27, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1000036
- Company Name: Product Quest Manufacturing LLC
- Inspection Date: 2017-01-27
- 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: 4

## Related Documents

- FDA Inspection 948191 - 2015-11-06
- [FDA Inspection 915252 - 2015-02-18](https://www.keypedia.com/records/fda_inspections/product-quest-manufacturing-llc/a416c0e2-9fc0-43dc-920f-18d4e360399d)
- FDA Inspection 771513 - 2012-03-11

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/product-quest-manufacturing-llc/36de467d-5619-4d92-800d-90b52d10ca1e

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