# FDA Inspection 539024 - Translite, LLC - October 03, 2008

Source: https://www.globalkeysolutions.net/records/fda_inspections/translite-llc/d9f9bdee-f426-4559-b75e-af53d9908a6e
Source feed: FDA_Inspections

> FDA Inspection 539024 for Translite, LLC on October 03, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 539024
- Company Name: Translite, LLC
- Inspection Date: 2008-10-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 539024 - 2008-10-03](https://www.globalkeysolutions.net/records/fda_inspections/translite-llc/6d5244e3-aaf8-4ae2-8979-50fa28611961)

Company: https://www.globalkeysolutions.net/companies/translite-llc/01e61609-a097-43c9-9c1e-fe997ad4fa11

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