FDA Inspection
Nustar IncNustar Inc – FDA Inspection, Sep 30, 2009
Record Details
This FDA Inspection record concerns Nustar Inc, with an inspection on September 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Nustar Inc
- Inspection Date
- September 30, 2009
- Product Type
- Devices
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ID · 4dcde8c3-332a-463d-8f88-31f70d86faa1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 615431
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)General
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Nustar Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 8, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Nustar Inc
- FDA Inspection 576262 - 2009-04-08
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