# FDA Inspection 1059989 - Altaravision, Inc. - March 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/altaravision-inc/3631b794-80da-42a3-b37f-b87aadf08ecc
Source feed: FDA_Inspections

> FDA Inspection 1059989 for Altaravision, Inc. on March 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059989
- Company Name: Altaravision, Inc.
- Inspection Date: 2018-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1059989 - 2018-03-20](https://www.keypedia.com/records/fda_inspections/altaravision-inc/763f1389-dc32-42cc-8cc4-05eda4369640)
- [FDA Inspection 927040 - 2015-05-13](https://www.keypedia.com/records/fda_inspections/altaravision-inc/8c0f88ff-154e-463b-b78f-5b20982925f8)
- [FDA Inspection 927040 - 2015-05-13](https://www.keypedia.com/records/fda_inspections/altaravision-inc/e4dc2943-b5df-493d-bacb-b273f57058f4)

Company: https://www.keypedia.com/companies/altaravision-inc/8852b0de-5489-45cb-8bfa-af35dc02b3a3

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