# Kulzer, LLC. – FDA Inspection, Jul 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/kulzer-llc/75779385-9f03-48a4-b562-03f7805082d9
Source feed: FDA_Inspections

> FDA inspection 1024387 of Kulzer, LLC., July 12, 2017. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024387
- Company Name: Kulzer, LLC.
- Inspection Date: 2017-07-12
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1120156 - 2018-10-12](https://www.keypedia.com/records/fda_inspections/kulzer-llc/9ebaf67d-ba1a-46a2-8e78-f58a0e8a2695)
- FDA Inspection 883853 - 2014-06-20
- [FDA Inspection 747015 - 2011-09-28](https://www.keypedia.com/records/fda_inspections/kulzer-llc/3cc587fc-25a6-499a-8cab-92fa71f44122)
- FDA Inspection 589433 - 2009-06-23

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/suyang-qin/c32419c5-1b78-4014-9f94-cb7ab17dfe05)

Company: https://www.keypedia.com/companies/kulzer-llc/35c53baa-9b43-462a-ab99-f4636a5dec03

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