# FDA Inspection 855042 - Rockford Specialties - November 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/rockford-specialties/1e6ded2e-08e3-46c9-9dbb-49d4d4eea875
Source feed: FDA_Inspections

> FDA Inspection 855042 for Rockford Specialties on November 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855042
- Company Name: Rockford Specialties
- Inspection Date: 2013-11-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1101646 - 2019-09-10](https://www.globalkeysolutions.net/records/fda_inspections/rockford-specialties/860098ca-5244-412e-9a86-8ae7362e863b)
- [FDA Inspection 855042 - 2013-11-12](https://www.globalkeysolutions.net/records/fda_inspections/rockford-specialties/92ec183a-eac1-4746-accb-78298c13bf8a)

Company: https://www.globalkeysolutions.net/companies/rockford-specialties/489395cc-debe-4021-b091-16aff7ec1e57

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