# Glytec, LLC. – FDA Inspection, Aug 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/glytec-llc/eaf4e739-07d7-44fd-b596-02a6343f7c15
Source feed: FDA_Inspections

> FDA inspection 989187 of Glytec, LLC., August 18, 2016. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989187
- Company Name: Glytec, LLC.
- Inspection Date: 2016-08-18
- 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: 0

## Related Documents

- FDA Inspection 1310522 - 2026-03-18

Company: https://www.keypedia.com/companies/glytec-llc/d8d3a5e3-729b-43a1-8452-ee2ac3315f9b

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