# FDA Inspection 1024105 - Molnlycke Manufacturing Us Llc - July 05, 2017

Source: https://www.keypedia.com/records/fda_inspections/molnlycke-manufacturing-us-llc/9595938e-8463-4118-92b3-084a00ed8199
Source feed: FDA_Inspections

> FDA Inspection 1024105 for Molnlycke Manufacturing Us Llc on July 05, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024105
- Company Name: Molnlycke Manufacturing Us Llc
- Inspection Date: 2017-07-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/molnlycke-manufacturing-us-llc/e7934299-1d6d-403c-9b07-1c630174c023

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