# FDA Inspection 719451 - Lockheed Martin Gyrocam Systems, Inc. - April 08, 2011

Source: https://www.keypedia.com/records/fda_inspections/lockheed-martin-gyrocam-systems-inc/908140ce-a9d5-428f-a12d-43a752875826
Source feed: FDA_Inspections

> FDA Inspection 719451 for Lockheed Martin Gyrocam Systems, Inc. on April 08, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 719451
- Company Name: Lockheed Martin Gyrocam Systems, Inc.
- Inspection Date: 2011-04-08
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 642342 - 2010-01-29](https://www.keypedia.com/records/fda_inspections/lockheed-martin-gyrocam-systems-inc/5c798c8f-a610-4a72-96b0-a52b49ba13e9)

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