# Saltillo Corporation – FDA Inspection, Sep 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/saltillo-corporation/beda015e-a47d-47c6-be96-5ab34f51d8b1
Source feed: FDA_Inspections

> FDA inspection 847810 of Saltillo Corporation, September 10, 2013. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 847810
- Company Name: Saltillo Corporation
- Inspection Date: 2013-09-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- [FDA Inspection 1073685 - 2018-12-06](https://www.keypedia.com/records/fda_inspections/saltillo-corporation/721ae4e8-bef9-4bdf-a28f-7564f12e240d)

Company: https://www.keypedia.com/companies/saltillo-corporation/7850626d-b9a1-41e6-88f1-7bad0e807337

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