# Gregory Manufacturing, Inc. – FDA Inspection, Sep 12, 2014

Source: https://www.keypedia.com/records/fda_inspections/gregory-manufacturing-inc/132bbec8-db4a-44fd-ac7a-8b46ff2f1bee
Source feed: FDA_Inspections

> FDA inspection 896691 of Gregory Manufacturing, Inc., September 12, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 896691
- Company Name: Gregory Manufacturing, Inc.
- Inspection Date: 2014-09-12
- 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 1311716 - 2026-04-02](https://www.keypedia.com/records/fda_inspections/gregory-manufacturing-inc/e37027a3-7122-406e-b7ac-79166c3818a9)
- FDA Inspection 1075004 - 2018-11-21
- FDA Inspection 747165 - 2011-09-21

Company: https://www.keypedia.com/companies/gregory-manufacturing-inc/1b81e669-eda5-4d5b-8be1-44bd3d264bb5

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