# Eisertech LLC – FDA Inspection, Sep 2, 2015

Source: https://www.keypedia.com/records/fda_inspections/eisertech-llc/bceedf41-5b7d-4e67-9ed6-504603f0b52f
Source feed: FDA_Inspections

> FDA inspection 941366 of Eisertech LLC, September 02, 2015. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 941366
- Company Name: Eisertech LLC
- Inspection Date: 2015-09-02
- 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: 7

## Related Documents

- [FDA Inspection 1100060 - 2019-08-21](https://www.keypedia.com/records/fda_inspections/eisertech-llc/fed9d684-55ec-46e1-a341-0849b7737d90)
- FDA Inspection 813940 - 2012-12-19

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

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