FDA Inspection
Lockheed Martin Gyrocam Systems, Inc.Lockheed Martin Gyrocam Systems, Inc. – FDA Inspection, Jan 29, 2010
Record Details
This FDA Inspection record concerns Lockheed Martin Gyrocam Systems, Inc., with an inspection on January 29, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 29, 2010
- Product Type
- Devices
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ID · 5c798c8f-a610-4a72-96b0-a52b49ba13e9
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 642342
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
7- 21 CFR 1040.10(f)(5)(iii)Emission indicator pre 8/20/86
- 21 CFR 1040.10(f)(2)(i)Safety interlock not provided
- 21 CFR 1040.10(f)(3)Remote interlock connector
- 21 CFR 1040.10(g)(10)Labels legible, visible, permanent
- 21 CFR 1040.10(e)(1)Certification tests inadequate
- 21 CFR 1002.13Failure to submit
- 21 CFR 1002.10Failure to submit, distinct marking
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Other FDA inspections of Lockheed Martin Gyrocam Systems, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 8, 2011 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Lockheed Martin Gyrocam Systems, Inc.
- FDA Inspection 719451 - 2011-04-08
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