# General Devices Llc – FDA Inspection, Jun 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/general-devices-llc/7240be77-4617-4f28-b5b6-ec17e8b25f48
Source feed: FDA_Inspections

> FDA inspection 931039 of General Devices Llc, June 11, 2015. Classification: Official Action Indicated (OAI). 3 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 931039
- Company Name: General Devices Llc
- Inspection Date: 2015-06-11
- 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: 3

## Related Documents

- FDA Inspection 1018328 - 2017-03-30
- FDA Inspection 812713 - 2012-12-14
- [FDA Inspection 678182 - 2010-07-29](https://www.keypedia.com/records/fda_inspections/general-devices-llc/dcf2dd96-0a03-42b5-ae17-1513dbcfd255)

Company: https://www.keypedia.com/companies/general-devices-llc/2ab2cc56-b870-4fc9-9a3f-f8bd76bc5cea

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