# FDA Inspection 980880 - Medivance Inc. - July 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/medivance-inc/1539ef9b-cfd7-4a73-9733-37ace71a5afa
Source feed: FDA_Inspections

> FDA Inspection 980880 for Medivance Inc. on July 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980880
- Company Name: Medivance Inc.
- Inspection Date: 2016-07-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 980880 - 2016-07-20](https://www.keypedia.com/records/fda_inspections/medivance-inc/725e1020-170a-405b-9da2-7388b8605f4b)
- [FDA Inspection 805531 - 2012-11-01](https://www.keypedia.com/records/fda_inspections/medivance-inc/1374c5e1-6e3c-47e5-b583-8abef716b868)
- [FDA Inspection 805531 - 2012-11-01](https://www.keypedia.com/records/fda_inspections/medivance-inc/3f107122-c9d4-4e22-9961-e4260c8ab85e)
- [FDA Inspection 556915 - 2009-01-16](https://www.keypedia.com/records/fda_inspections/medivance-inc/5db24fcc-c221-4551-a714-6b74681ebd56)

Company: https://www.keypedia.com/companies/medivance-inc/e20b9be1-f956-49fa-b4cd-56e15fbca716

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