# Glasir Medical, LP – FDA Inspection, Jun 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/glasir-medical-lp/ad73c6ad-a226-44ce-8f5c-6ff43ba1a946
Source feed: FDA_Inspections

> FDA inspection 1016248 of Glasir Medical, LP, June 28, 2017. Classification: Voluntary Action Indicated (VAI). 13 citations under 21 CFR parts 803, 820 and 1271. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016248
- Company Name: Glasir Medical, LP
- Inspection Date: 2017-06-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 13

## Related Documents

- [FDA Inspection 821991 - 2013-03-20](https://www.keypedia.com/records/fda_inspections/glasir-medical-lp/9c886cc9-09c5-4e86-948b-8eaa5d241b57)
- [FDA Inspection 769845 - 2012-02-29](https://www.keypedia.com/records/fda_inspections/glasir-medical-lp/7041f7e4-de00-4b10-a01e-10b0f7734536)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/iris-c-macinnes/5e8d7fef-18d5-453d-82b2-19e8e2897d26)

Company: https://www.keypedia.com/companies/glasir-medical-lp/c85030d0-5bed-437c-9de2-d32da9d6552e

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