# FDA Inspection 777205 - Orbital Technologies Corporation (Orbitec) - April 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/orbital-technologies-corporation-orbitec/be39872c-a716-4e8a-ad8a-8c8cbb5ec0e9
Source feed: FDA_Inspections

> FDA Inspection 777205 for Orbital Technologies Corporation (Orbitec) on April 06, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 777205
- Company Name: Orbital Technologies Corporation (Orbitec)
- Inspection Date: 2012-04-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 576162 - 2009-04-13](https://www.keypedia.com/records/fda_inspections/orbital-technologies-corporation-orbitec/aadc98b1-55e2-4e06-beb2-0ae93d1ca008)

Company: https://www.keypedia.com/companies/orbital-technologies-corporation-orbitec/bd4329d7-b4f3-4814-852d-7d6b6b96689c

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