# OndaMed Inc – FDA Inspection, Aug 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/ondamed-inc/10f3baf8-1177-4a70-91e2-a5966d5221ff
Source feed: FDA_Inspections

> FDA inspection 986755 of OndaMed Inc, August 15, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 986755
- Company Name: OndaMed Inc
- Inspection Date: 2016-08-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1067339 - 2018-09-28](https://www.keypedia.com/records/fda_inspections/ondamed-inc/a9c51805-ec82-4916-abaf-df1b4f7966b2)
- FDA Inspection 938468 - 2015-08-17

Company: https://www.keypedia.com/companies/ondamed-inc/fe0ea238-d61c-4acd-b986-5a9da81bd84c

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