# FDA Inspection 709989 - Intravena, LLC - February 17, 2011

Source: https://www.keypedia.com/records/fda_inspections/intravena-llc/71f4e16f-5227-45aa-8348-92e8b02afcf3
Source feed: FDA_Inspections

> FDA Inspection 709989 for Intravena, LLC on February 17, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 709989
- Company Name: Intravena, LLC
- Inspection Date: 2011-02-17
- 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 709989 - 2011-02-17](https://www.keypedia.com/records/fda_inspections/intravena-llc/8eb3afd3-2d35-42c5-9937-a6ad50dd01ce)

Company: https://www.keypedia.com/companies/intravena-llc/f8ccde44-ad44-4811-8fa2-7e6a32068621

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