# Lonza Walkersville, Inc. – FDA Inspection, Jul 3, 2018

Source: https://www.keypedia.com/records/fda_inspections/lonza-walkersville-inc/b8e95b40-13a8-4dff-a74a-834c5ac2837c
Source feed: FDA_Inspections

> FDA inspection 1058040 of Lonza Walkersville, Inc., July 03, 2018. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058040
- Company Name: Lonza Walkersville, Inc.
- Inspection Date: 2018-07-03
- 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: 4

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- FDA Inspection 991587 - 2016-06-09

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)

Company: https://www.keypedia.com/companies/lonza-walkersville-inc/5008199b-623e-432c-942c-db06b6333f53

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