# FDA Inspection 642342 - Lockheed Martin Gyrocam Systems, Inc. - January 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/lockheed-martin-gyrocam-systems-inc/5c798c8f-a610-4a72-96b0-a52b49ba13e9
Source feed: FDA_Inspections

> FDA Inspection 642342 for Lockheed Martin Gyrocam Systems, Inc. on January 29, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 642342
- Company Name: Lockheed Martin Gyrocam Systems, Inc.
- Inspection Date: 2010-01-29
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 719451 - 2011-04-08](https://www.keypedia.com/records/fda_inspections/lockheed-martin-gyrocam-systems-inc/908140ce-a9d5-428f-a12d-43a752875826)

Company: https://www.keypedia.com/companies/lockheed-martin-gyrocam-systems-inc/4ea9571e-c035-4e14-9493-1dc09c92dbcf

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