# FDA Inspection 916761 - Gelflex Laboratories - January 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/gelflex-laboratories/240a7308-5f31-4e1e-8f50-7071b38b3f12
Source feed: FDA_Inspections

> FDA Inspection 916761 for Gelflex Laboratories on January 30, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916761
- Company Name: Gelflex Laboratories
- Inspection Date: 2015-01-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 916761 - 2015-01-30](https://www.keypedia.com/records/fda_inspections/gelflex-laboratories/c4345ece-9b1c-4817-b5d4-f62f8cf1b90c)

Company: https://www.keypedia.com/companies/gelflex-laboratories/c780b470-5359-47ca-92aa-7530ea259f8c

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