FDA Inspection
Intermed Group, Inc.Intermed Group, Inc. – FDA Inspection, Sep 18, 2014
Record Details
This FDA Inspection record concerns Intermed Group, Inc., with an inspection on September 18, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Intermed Group, Inc.
- Inspection Date
- September 18, 2014
- Product Type
- Devices
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ID · 1258a0a7-72e1-4740-b699-d113075ce24c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896205
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.20(d)Quality plan
- 21 CFR 820.22Quality Audit/Reaudit - conducted
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Other FDA inspections of Intermed Group, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 15, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Intermed Group, Inc.
- FDA Inspection 754773 - 2011-11-15
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