FDA Inspection
InteloMed, Inc.InteloMed, Inc. – FDA Inspection, Feb 28, 2017
Record Details
This FDA Inspection record concerns InteloMed, Inc., with an inspection on February 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 544311b4-d4fb-4d21-a4b5-1dcbbebe1358
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1012237
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of InteloMed, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 15, 2020 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for InteloMed, Inc.
- FDA Inspection 1117890 - 2020-01-15
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