# FDA Inspection 746726 - Dwyer Precision Products, Inc. - September 20, 2011

Source: https://www.keypedia.com/records/fda_inspections/dwyer-precision-products-inc/e7e0ae2d-2753-4732-a37e-d87728cbb644
Source feed: FDA_Inspections

> FDA Inspection 746726 for Dwyer Precision Products, Inc. on September 20, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 746726
- Company Name: Dwyer Precision Products, Inc.
- Inspection Date: 2011-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 746726 - 2011-09-20](https://www.keypedia.com/records/fda_inspections/dwyer-precision-products-inc/513c3e5a-cc86-4f6d-9343-84227303c50f)

Company: https://www.keypedia.com/companies/dwyer-precision-products-inc/32302fb3-e53a-49da-95f6-aba9fe685602

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