# FDA Inspection 821233 - Prentke Romich Company DBA PRC-Saltillo - February 15, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/98f21f30-b3b0-4563-96f7-4e85a1b92a1c
Source feed: FDA_Inspections

> FDA Inspection 821233 for Prentke Romich Company DBA PRC-Saltillo on February 15, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 821233
- Company Name: Prentke Romich Company DBA PRC-Saltillo
- Inspection Date: 2013-02-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1268699 - 2025-05-01](https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/82765ad1-bffc-479a-8e4c-5b293f54652c)
- [FDA Inspection 1268699 - 2025-05-01](https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/1015f06d-caf6-415a-95a4-b4f6cdcc52cc)
- [FDA Inspection 1268699 - 2025-05-01](https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/a8890111-2d5b-4fcf-984c-89844647a7d2)
- [FDA Inspection 1268699 - 2025-05-01](https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/d0ebc425-3880-4450-9055-ed9d83306a3f)
- [FDA Inspection 1073686 - 2018-12-04](https://www.globalkeysolutions.net/records/fda_inspections/prentke-romich-company-dba-prc-saltillo/6c6c6b23-0b8d-4612-aa6d-f3aeddd480e3)

Company: https://www.globalkeysolutions.net/companies/prentke-romich-company-dba-prc-saltillo/bf155ced-53bb-41e3-9409-c14b0aa3a078

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