# FDA Inspection 1100060 - Eisertech LLC - August 21, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/eisertech-llc/fed9d684-55ec-46e1-a341-0849b7737d90/
Source feed: FDA_Inspections

> FDA Inspection 1100060 for Eisertech LLC on August 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100060
- Company Name: Eisertech LLC
- Inspection Date: 2019-08-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100060 - 2019-08-21](https://www.globalkeysolutions.net/api/records/fda_inspections/eisertech-llc/d2e6e7b9-5c66-42e9-9b42-b2bd0fc4f519/)
- [FDA Inspection 941366 - 2015-09-02](https://www.globalkeysolutions.net/api/records/fda_inspections/eisertech-llc/bceedf41-5b7d-4e67-9ed6-504603f0b52f/)
- [FDA Inspection 813940 - 2012-12-19](https://www.globalkeysolutions.net/api/records/fda_inspections/eisertech-llc/fa5b6021-bfc3-4530-a8fe-563dabea9ce9/)
- [FDA Inspection 813940 - 2012-12-19](https://www.globalkeysolutions.net/api/records/fda_inspections/eisertech-llc/c52c8678-5ecc-4346-9375-a13326619772/)

Company: https://www.globalkeysolutions.net/companies/eisertech-llc/4a496f99-fb06-4cfe-b213-91cbc640aad2

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