# Repro Parts, Inc. – FDA Inspection, Dec 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 of Repro Parts, Inc., December 18, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 907142
- Company Name: Repro Parts, Inc.
- Inspection Date: 2014-12-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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