# FDA Inspection 604793 - Lowell General Hospital/IRB - August 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/lowell-general-hospitalirb/8883b43f-1270-469c-b70d-d3557d53f29a
Source feed: FDA_Inspections

> FDA Inspection 604793 for Lowell General Hospital/IRB on August 11, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 604793
- Company Name: Lowell General Hospital/IRB
- Inspection Date: 2009-08-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 920098 - 2015-03-11](https://www.keypedia.com/records/fda_inspections/lowell-general-hospitalirb/88ab34fc-9a7c-4197-ae89-23a0bab07425)
- [FDA Inspection 920098 - 2015-03-11](https://www.keypedia.com/records/fda_inspections/lowell-general-hospitalirb/0968ba3c-1b29-4cad-a5da-dac15b2c275a)

Company: https://www.keypedia.com/companies/lowell-general-hospitalirb/de71969e-2d0a-4c39-bd76-902cec07e16e

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