# FDA Inspection 705350 - Kegelmaster, Inc. - January 07, 2011

Source: https://www.keypedia.com/records/fda_inspections/kegelmaster-inc/6aeec2e8-d6f7-4ac5-9196-d3b0544edeb9
Source feed: FDA_Inspections

> FDA Inspection 705350 for Kegelmaster, Inc. on January 07, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 705350
- Company Name: Kegelmaster, Inc.
- Inspection Date: 2011-01-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 966754 - 2016-02-09](https://www.keypedia.com/records/fda_inspections/kegelmaster-inc/6020ab41-6427-479f-89bd-effdef12b895)
- [FDA Inspection 966754 - 2016-02-09](https://www.keypedia.com/records/fda_inspections/kegelmaster-inc/c1982a37-ef2e-451c-b415-f1b0649168c7)
- [FDA Inspection 705350 - 2011-01-07](https://www.keypedia.com/records/fda_inspections/kegelmaster-inc/e27805e4-1d2a-4dab-844c-e777fe062c51)

Company: https://www.keypedia.com/companies/kegelmaster-inc/a5e0f69c-914b-4d7b-a480-3c4f7434e845

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