# Summit Industries Inc. – FDA Inspection, May 29, 2012

Source: https://www.keypedia.com/records/fda_inspections/summit-industries-inc/e2651b28-5831-4fea-b0a1-3adbc49242e8
Source feed: FDA_Inspections

> FDA inspection 787439 of Summit Industries Inc., May 29, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 787439
- Company Name: Summit Industries Inc.
- Inspection Date: 2012-05-29
- 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: 5

## Related Documents

- [FDA Inspection 1264391 - 2025-03-20](https://www.keypedia.com/records/fda_inspections/summit-industries-inc/3d348bac-9141-4178-8c28-fac346829a42)
- FDA Inspection 1180911 - 2022-09-30
- [FDA Inspection 1027765 - 2017-09-29](https://www.keypedia.com/records/fda_inspections/summit-industries-inc/cb347ff4-f1b8-4e9f-9700-aa0654925b18)
- FDA Inspection 838805 - 2013-07-02
- FDA Inspection 546595 - 2008-11-10

Company: https://www.keypedia.com/companies/summit-industries-inc/f2e172b5-3734-481d-85d4-5258a68dd2be

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