# FDA Inspection 907142 - Repro Parts, Inc. - December 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/repro-parts-inc/a0d8d7c3-431b-4860-b9f7-03c1a25aec56
Source feed: FDA_Inspections

> FDA Inspection 907142 for Repro Parts, Inc. on December 18, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907142
- Company Name: Repro Parts, Inc.
- Inspection Date: 2014-12-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 907142 - 2014-12-18](https://www.keypedia.com/records/fda_inspections/repro-parts-inc/874335e9-581c-446c-bdba-de2d198a21ac)

Company: https://www.keypedia.com/companies/repro-parts-inc/da7a489c-560d-41cc-b71c-36c49cf3c53c

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