# FDA Inspection 1065416 - Molnlycke Manufacturing US, Llc - August 30, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/molnlycke-manufacturing-us-llc/e6e104b8-5773-4989-b101-67bd73bc7949
Source feed: FDA_Inspections

> FDA Inspection 1065416 for Molnlycke Manufacturing US, Llc on August 30, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065416
- Company Name: Molnlycke Manufacturing US, Llc
- Inspection Date: 2018-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1065416 - 2018-08-30](https://www.globalkeysolutions.net/records/fda_inspections/molnlycke-manufacturing-us-llc/d649395c-23e7-4486-bb0e-15ca8c2e509a)

Company: https://www.globalkeysolutions.net/companies/molnlycke-manufacturing-us-llc/07ed9457-21af-4edb-bb19-05b6a4a710a6

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