# Repro-Med Systems, Inc. – FDA Inspection, Jun 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/f30e24d8-0d40-417a-8e4c-2fdfc24950db
Source feed: FDA_Inspections

> FDA inspection 929452 of Repro-Med Systems, Inc., June 23, 2015. Classification: Official Action Indicated (OAI). 15 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 929452
- Company Name: Repro-Med Systems, Inc.
- Inspection Date: 2015-06-23
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 15

## Related Documents

- [FDA Inspection 1029627 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/b794adc6-ca44-4acb-9efa-3ba57d3934bf)
- [FDA Inspection 996093 - 2016-12-16](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/ca0b7afe-57e2-43ac-8005-9591400d9a99)
- FDA Inspection 793650 - 2012-07-20
- FDA Inspection 683171 - 2010-09-21
- FDA Inspection 627589 - 2009-10-28

Company: https://www.keypedia.com/companies/repro-med-systems-inc/33ca025a-ec91-4b0c-ae99-ac661170de7e

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