# FDA Inspection 962618 - MaineHealth IRB #1 - March 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/92aea296-b668-4a49-962b-74e328c3f53a
Source feed: FDA_Inspections

> FDA Inspection 962618 for MaineHealth IRB #1 on March 16, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 962618
- Company Name: MaineHealth IRB #1
- Inspection Date: 2016-03-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1167287 - 2022-03-24](https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/0ab208b1-8993-4a33-bcec-cb68f58d90f4)
- [FDA Inspection 1167287 - 2022-03-24](https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/1232224d-85d0-4941-b7d3-a2e7a18af5b2)
- [FDA Inspection 1167287 - 2022-03-24](https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/64240d8e-6e2c-4d96-9fdd-6fa7d6a3ded6)
- [FDA Inspection 962618 - 2016-03-16](https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/03fef64a-95e6-4625-b389-9f378063b660)
- [FDA Inspection 648126 - 2010-02-12](https://www.keypedia.com/records/fda_inspections/mainehealth-irb-1/0c017c6f-fb47-4ebc-85d6-1770c8ad741a)

Company: https://www.keypedia.com/companies/mainehealth-irb-1/c20e5d7b-a543-410b-b31e-2db3cea4f2ad

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