# FDA Inspection 987721 - Kulzer SRL - September 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/kulzer-srl/b9a8b889-0782-455b-8da5-2f7f8ee449ec
Source feed: FDA_Inspections

> FDA Inspection 987721 for Kulzer SRL on September 15, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987721
- Company Name: Kulzer SRL
- Inspection Date: 2016-09-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1081761 - 2019-02-13](https://www.keypedia.com/records/fda_inspections/kulzer-srl/fa0da22e-8005-4225-9208-66ffedda936c)

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