# Alto Development Corp. – FDA Inspection, Jun 28, 2018

Source: https://www.keypedia.com/records/fda_inspections/alto-development-corp/38f3c865-4187-4ad7-8f41-000e6f21c0b0
Source feed: FDA_Inspections

> FDA inspection 1057213 of Alto Development Corp., June 28, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057213
- Company Name: Alto Development Corp.
- Inspection Date: 2018-06-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 928537 - 2015-05-29
- FDA Inspection 815110 - 2013-01-28
- FDA Inspection 647323 - 2010-03-01

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/william-r-chang/67893bac-29e2-45b4-ba2c-1ef548781b9c)

Company: https://www.keypedia.com/companies/alto-development-corp/d8d2db53-a59d-4094-9c70-0c504537cc59

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7