# FDA Inspection 1029627 - Repro-Med Systems, Inc. - October 19, 2017

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

> FDA Inspection 1029627 for Repro-Med Systems, Inc. on October 19, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029627 - 2017-10-19](https://www.globalkeysolutions.net/records/fda_inspections/repro-med-systems-inc/b278a98f-1b2d-4816-a28b-03b7d9064473)
- [FDA Inspection 996093 - 2016-12-16](https://www.globalkeysolutions.net/records/fda_inspections/repro-med-systems-inc/0ac00916-4fe9-4b11-bf62-d3a8ef4a40e1)
- [FDA Inspection 996093 - 2016-12-16](https://www.globalkeysolutions.net/records/fda_inspections/repro-med-systems-inc/ca0b7afe-57e2-43ac-8005-9591400d9a99)
- [FDA Inspection 929452 - 2015-06-23](https://www.globalkeysolutions.net/records/fda_inspections/repro-med-systems-inc/a302eb26-b1cb-42c4-a720-f7bac8985b2d)
- [FDA Inspection 929452 - 2015-06-23](https://www.globalkeysolutions.net/records/fda_inspections/repro-med-systems-inc/f30e24d8-0d40-417a-8e4c-2fdfc24950db)

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

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