# FDA Inspection 1030070 - IVWATCH, LLC - August 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/ivwatch-llc/ed4d9a7a-467d-4847-bc50-522f6d6391e4
Source feed: FDA_Inspections

> FDA Inspection 1030070 for IVWATCH, LLC on August 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030070
- Company Name: IVWATCH, LLC
- Inspection Date: 2017-08-25
- 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 1030070 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/ivwatch-llc/683494cb-b78c-4561-b9ef-a5c190db29a8)

Company: https://www.keypedia.com/companies/ivwatch-llc/c08f7cdf-b294-42ca-b9a4-76cd3fe467f2

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