# FH INDUSTRIE – FDA Inspection, Sep 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/fh-industrie/1decea7a-37fa-40d0-88e7-7f6f87404e49
Source feed: FDA_Inspections

> FDA inspection 1064620 of FH INDUSTRIE, September 06, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064620
- Company Name: FH INDUSTRIE
- Inspection Date: 2018-09-06
- 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

## Related Documents

- FDA Inspection 1273707 - 2025-05-19
- [FDA Inspection 940386 - 2015-07-23](https://www.keypedia.com/records/fda_inspections/fh-industrie/b2a2c57d-8654-4573-b795-6631ef877601)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-j-gasparovich/478888db-d4b3-481a-89f5-ee234a160f07)

Company: https://www.keypedia.com/companies/fh-industrie/b94b0182-e20c-4adf-8e44-b5b1c04d0c08

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