# FDA Inspection 613324 - Munroe Regional Medical Center Clinical Laboratory - September 21, 2009

Source: https://www.keypedia.com/records/fda_inspections/munroe-regional-medical-center-clinical-laboratory/80f2d0c4-e3be-4beb-8836-578f27c50585
Source feed: FDA_Inspections

> FDA Inspection 613324 for Munroe Regional Medical Center Clinical Laboratory on September 21, 2009. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 613324
- Company Name: Munroe Regional Medical Center Clinical Laboratory
- Inspection Date: 2009-09-21
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 944907 - 2015-10-02](https://www.keypedia.com/records/fda_inspections/munroe-regional-medical-center-clinical-laboratory/5c6c40f2-57cf-4f8b-b51d-b7e7abcb8eae)
- [FDA Inspection 613324 - 2009-09-21](https://www.keypedia.com/records/fda_inspections/munroe-regional-medical-center-clinical-laboratory/32585924-4a82-45ac-96b2-f7fdd5d5f568)

Company: https://www.keypedia.com/companies/munroe-regional-medical-center-clinical-laboratory/e03efd1e-0213-456d-b19b-4717eebad287

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