# FDA Inspection 800522 - Welch Allyn Protocol, Inc - September 26, 2012

Source: https://www.keypedia.com/records/fda_inspections/welch-allyn-protocol-inc/ba60a8fa-8f9c-4e27-8c0f-885cbc22853d
Source feed: FDA_Inspections

> FDA Inspection 800522 for Welch Allyn Protocol, Inc on September 26, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 800522
- Company Name: Welch Allyn Protocol, Inc
- Inspection Date: 2012-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 800522 - 2012-09-26](https://www.keypedia.com/records/fda_inspections/welch-allyn-protocol-inc/f1a9d876-e046-452f-8900-2306ac44a19e)
- [FDA Inspection 559947 - 2009-01-29](https://www.keypedia.com/records/fda_inspections/welch-allyn-protocol-inc/b11553b4-9de1-4bbb-bcd5-50dd4b1e5cae)
- [FDA Inspection 541385 - 2008-10-06](https://www.keypedia.com/records/fda_inspections/welch-allyn-protocol-inc/1aca5317-fbf7-42a9-a823-1054de8c3ffd)
- [FDA Inspection 541385 - 2008-10-06](https://www.keypedia.com/records/fda_inspections/welch-allyn-protocol-inc/2f2d3301-02e6-4969-b8cc-21a443799a6a)

Company: https://www.keypedia.com/companies/welch-allyn-protocol-inc/8a320db9-7178-4bd4-b387-dc89a1df6cfc

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