FDA Inspection
Omnitech Systems, Inc.Omnitech Systems, Inc. – FDA Inspection, Feb 3, 2010
Record Details
This FDA Inspection record concerns Omnitech Systems, Inc., with an inspection on February 3, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Omnitech Systems, Inc.
- Inspection Date
- February 3, 2010
- Product Type
- Devices
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ID · bf19ac3a-3ede-47f1-8891-993bda5385b8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 643042
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
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Other FDA inspections of Omnitech Systems, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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