# Kulzer SRL – FDA Inspection, Feb 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/kulzer-srl/fa0da22e-8005-4225-9208-66ffedda936c
Source feed: FDA_Inspections

> FDA inspection 1081761 of Kulzer SRL, February 13, 2019. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1081761
- Company Name: Kulzer SRL
- Inspection Date: 2019-02-13
- 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: 0

## Related Documents

- FDA Inspection 987721 - 2016-09-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/kulzer-srl/ab2c3df4-20a8-4697-ab5b-ba01df0f4ae5

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