# LOHMAN TECHNOLOGIES LLC – FDA Inspection, Feb 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/lohman-technologies-llc/5ada4efb-a3cf-4941-988f-275f06584a9f
Source feed: FDA_Inspections

> FDA inspection 1079151 of LOHMAN TECHNOLOGIES LLC, February 08, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079151
- Company Name: LOHMAN TECHNOLOGIES LLC
- Inspection Date: 2019-02-08
- 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: 2

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- [FDA Inspection 1250230 - 2024-09-27](https://www.keypedia.com/records/fda_inspections/lohman-technologies-llc/ca0299d2-1312-4469-9929-51ae47e9a1e5)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michelle-j-glembin/e58f4652-d09f-41a7-941d-335c7b5338ad)

Company: https://www.keypedia.com/companies/lohman-technologies-llc/b7f4762c-5899-43dd-9ee5-cd49f1cc7301

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