# FDA Inspection 929452 - Repro-Med Systems, Inc. - June 23, 2015

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

> FDA Inspection 929452 for Repro-Med Systems, Inc. on June 23, 2015. Classification: Official Action Indicated (OAI).

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

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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