FDA Inspection
Alto Development Corp.Alto Development Corp. – FDA Inspection, Jun 28, 2018
Record Details
This FDA Inspection record concerns Alto Development Corp., with an inspection on June 28, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 38f3c865-4187-4ad7-8f41-000e6f21c0b0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1057213
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
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Other FDA inspections of Alto Development Corp.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 29, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 28, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 1, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Alto Development Corp.
- FDA Inspection 928537 - 2015-05-29
- FDA Inspection 815110 - 2013-01-28
- FDA Inspection 647323 - 2010-03-01
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