# Saltillo Corporation – FDA Inspection, Dec 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/saltillo-corporation/721ae4e8-bef9-4bdf-a28f-7564f12e240d
Source feed: FDA_Inspections

> FDA inspection 1073685 of Saltillo Corporation, December 06, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073685
- Company Name: Saltillo Corporation
- Inspection Date: 2018-12-06
- 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: 2

## Related Documents

- [FDA Inspection 847810 - 2013-09-10](https://www.keypedia.com/records/fda_inspections/saltillo-corporation/beda015e-a47d-47c6-be96-5ab34f51d8b1)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

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