FDA Inspection
AstroNovaAstroNova – FDA Inspection, Jul 19, 2013
Record Details
This FDA Inspection record concerns AstroNova, with an inspection on July 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- AstroNova
- Inspection Date
- July 19, 2013
- Product Type
- Devices
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ID · 806ad3f5-f3d5-43c1-ac80-ad2258eaf5c1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 845318
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 803.56Submission of Supplement to Individual Report Within One Month
- 21 CFR 820.198(a)Complaints
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Other FDA inspections of AstroNova
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 25, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for AstroNova
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