FDA Inspection
Exel, Inc.Exel, Inc. – FDA Inspection, Feb 21, 2013
Record Details
This FDA Inspection record concerns Exel, Inc., with an inspection on February 21, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Exel, Inc.
- Inspection Date
- February 21, 2013
- Product Type
- Devices
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ID · fb2eb334-68f9-4f96-b9e3-b6672c3aaa7d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 821656
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.160(a)Lack of or inadequate procedures for distribution
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Exel, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 6, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Exel, Inc.
- FDA Inspection 640742 - 2010-01-06
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