# FDA Inspection 1073685 - Saltillo Corporation - December 06, 2018

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

> FDA Inspection 1073685 for Saltillo Corporation on December 06, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1073685 - 2018-12-06](https://www.globalkeysolutions.net/records/fda_inspections/saltillo-corporation/52f61a38-0a39-4ab6-af63-a33a86d8820e)
- [FDA Inspection 847810 - 2013-09-10](https://www.globalkeysolutions.net/records/fda_inspections/saltillo-corporation/1f1b516b-d421-4aa5-923b-773b4e93b1c3)
- [FDA Inspection 847810 - 2013-09-10](https://www.globalkeysolutions.net/records/fda_inspections/saltillo-corporation/beda015e-a47d-47c6-be96-5ab34f51d8b1)

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

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