# FDA Inspection 613787 - B & L Engineering - July 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/b-l-engineering/f5f0f0c9-0136-4362-b56e-75a702121e48
Source feed: FDA_Inspections

> FDA Inspection 613787 for B & L Engineering on July 30, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 613787
- Company Name: B & L Engineering
- Inspection Date: 2009-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 869377 - 2014-03-10](https://www.keypedia.com/records/fda_inspections/b-l-engineering/91a5dddf-be11-4d08-8477-3783fa3ccfd3)

Company: https://www.keypedia.com/companies/b-l-engineering/cf0f321f-6b09-4a9a-aae5-0dff562f7dd1

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