# FDA Inspection 845318 - AstroNova - July 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/astronova/6d089bf8-bc61-46b3-8da8-cc79e64c0978
Source feed: FDA_Inspections

> FDA Inspection 845318 for AstroNova on July 19, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 845318
- Company Name: AstroNova
- Inspection Date: 2013-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 845318 - 2013-07-19](https://www.keypedia.com/records/fda_inspections/astronova/806ad3f5-f3d5-43c1-ac80-ad2258eaf5c1)
- [FDA Inspection 712990 - 2011-02-25](https://www.keypedia.com/records/fda_inspections/astronova/ac617d7e-9f09-4612-a5b5-5125574bcb20)

Company: https://www.keypedia.com/companies/astronova/ddd7d21d-8592-4814-84d7-22f89184e347

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