FDA Inspection
Orbital Technologies Corporation (Orbitec)Orbital Technologies Corporation (Orbitec) – FDA Inspection, Apr 6, 2012
Record Details
This FDA Inspection record concerns Orbital Technologies Corporation (Orbitec), with an inspection on April 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- April 6, 2012
- Product Type
- Devices
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ID · be39872c-a716-4e8a-ad8a-8c8cbb5ec0e9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 777205
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.25(b)Training records
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Orbital Technologies Corporation (Orbitec)
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 13, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Orbital Technologies Corporation (Orbitec)
- FDA Inspection 576162 - 2009-04-13
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