# FDA Inspection 1089894 - Medco Manufacturing - May 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/medco-manufacturing/3d36937b-e834-4e4c-a38e-176c1c807e75
Source feed: FDA_Inspections

> FDA Inspection 1089894 for Medco Manufacturing on May 13, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089894
- Company Name: Medco Manufacturing
- Inspection Date: 2019-05-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1089894 - 2019-05-13](https://www.keypedia.com/records/fda_inspections/medco-manufacturing/1e85a10f-5249-4477-bb25-10fa998a7617)
- [FDA Inspection 566508 - 2009-02-26](https://www.keypedia.com/records/fda_inspections/medco-manufacturing/e019e4b0-b250-4b96-8603-b66cfebe18e2)

Company: https://www.keypedia.com/companies/medco-manufacturing/3dbeb100-78b8-4035-9c32-dc9b63391793

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