# FDA Inspection 896189 - N. M. Beale Company, Inc. - September 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/n-m-beale-company-inc/46007914-c6cd-40f5-9da7-61ab73670bd5
Source feed: FDA_Inspections

> FDA Inspection 896189 for N. M. Beale Company, Inc. on September 18, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 896189
- Company Name: N. M. Beale Company, Inc.
- Inspection Date: 2014-09-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 896189 - 2014-09-18](https://www.keypedia.com/records/fda_inspections/n-m-beale-company-inc/a28eaab5-6854-419a-a6de-93ea0a25a6b7)
- [FDA Inspection 763281 - 2012-01-18](https://www.keypedia.com/records/fda_inspections/n-m-beale-company-inc/4b57b80f-a0af-4c9b-be80-141df5e9e9c5)
- [FDA Inspection 550609 - 2008-10-22](https://www.keypedia.com/records/fda_inspections/n-m-beale-company-inc/7bb52741-eab5-4543-b5b7-6f8d1fa7462c)

Company: https://www.keypedia.com/companies/n-m-beale-company-inc/00246d66-1565-4508-915f-8c7163510587

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