# FDA Inspection 857943 - Armedica Manufacturing Corp - December 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/armedica-manufacturing-corp/f0fac8f1-4c46-44af-a2e4-95d3c4245654
Source feed: FDA_Inspections

> FDA Inspection 857943 for Armedica Manufacturing Corp on December 05, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857943
- Company Name: Armedica Manufacturing Corp
- Inspection Date: 2013-12-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 857943 - 2013-12-05](https://www.keypedia.com/records/fda_inspections/armedica-manufacturing-corp/2b08c9b8-6aa7-4ee5-9a72-0732aa5b11ae)
- [FDA Inspection 713387 - 2011-03-10](https://www.keypedia.com/records/fda_inspections/armedica-manufacturing-corp/8eab406b-5191-47a6-a858-129c68eb49a7)
- [FDA Inspection 713387 - 2011-03-10](https://www.keypedia.com/records/fda_inspections/armedica-manufacturing-corp/d61698e3-a450-4bc1-a3f1-45433ce79e9c)

Company: https://www.keypedia.com/companies/armedica-manufacturing-corp/794c2a38-4bda-47bb-9a03-efc90093312d

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