FDA Inspection
VIDAR Systems CorpVIDAR Systems Corp – FDA Inspection, Aug 29, 2012
Record Details
This FDA Inspection record concerns VIDAR Systems Corp, with an inspection on August 29, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- VIDAR Systems Corp
- Inspection Date
- August 29, 2012
- Product Type
- Devices
View Company Profile
ID · a16c1c65-bc64-4e9d-8a04-e3811e5257f3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 798394
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(g)Design validation - documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of VIDAR Systems Corp
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 8, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 21, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 11, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 21, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for VIDAR Systems Corp
- FDA Inspection 1155929 - 2021-10-08
- FDA Inspection 1068361 - 2018-09-21
- FDA Inspection 930039 - 2015-06-11
- FDA Inspection 735684 - 2011-07-21
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