# Repro-Med Systems, Inc. – FDA Inspection, Oct 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/b794adc6-ca44-4acb-9efa-3ba57d3934bf
Source feed: FDA_Inspections

> FDA inspection 1029627 of Repro-Med Systems, Inc., October 19, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029627
- Company Name: Repro-Med Systems, Inc.
- Inspection Date: 2017-10-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 996093 - 2016-12-16](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/ca0b7afe-57e2-43ac-8005-9591400d9a99)
- [FDA Inspection 929452 - 2015-06-23](https://www.keypedia.com/records/fda_inspections/repro-med-systems-inc/f30e24d8-0d40-417a-8e4c-2fdfc24950db)
- FDA Inspection 793650 - 2012-07-20
- FDA Inspection 683171 - 2010-09-21
- FDA Inspection 627589 - 2009-10-28

## Related Officers

- Issuing Officer

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