# FDA Inspection 944001 - Davis Schottlander and Davis, Ltd. - September 24, 2015

Source: https://www.keypedia.com/records/fda_inspections/davis-schottlander-and-davis-ltd/154d7a95-e5eb-46a7-866b-577506fa9f5f
Source feed: FDA_Inspections

> FDA Inspection 944001 for Davis Schottlander and Davis, Ltd. on September 24, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 944001
- Company Name: Davis Schottlander and Davis, Ltd.
- Inspection Date: 2015-09-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 944001 - 2015-09-24](https://www.keypedia.com/records/fda_inspections/davis-schottlander-and-davis-ltd/e9ae3127-01f3-447e-b77c-0458dccfb1af)
- [FDA Inspection 665098 - 2010-06-03](https://www.keypedia.com/records/fda_inspections/davis-schottlander-and-davis-ltd/d0a804cb-f30b-4af7-951e-b52c2a63ed97)

Company: https://www.keypedia.com/companies/davis-schottlander-and-davis-ltd/f49197ad-c492-4819-847a-b25c5ae62a93

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