# Sypris Electronics Llc – FDA Inspection, Jun 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/sypris-electronics-llc/ed04007b-41cd-4c76-9ca9-59a33560796b
Source feed: FDA_Inspections

> FDA inspection 1093280 of Sypris Electronics Llc, June 14, 2019. Classification: No Action Indicated (NAI). 7 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: 1093280
- Company Name: Sypris Electronics Llc
- Inspection Date: 2019-06-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1215825 - 2023-08-16

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/sypris-electronics-llc/faeb4164-7db8-4f53-a264-c0a7ea7d4049

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