# FDA Inspection 994691 - Lundell Manufacturing Corp - November 16, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/lundell-manufacturing-corp/df90ffc9-705e-4da6-854c-a274d02d7eb2
Source feed: FDA_Inspections

> FDA Inspection 994691 for Lundell Manufacturing Corp on November 16, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994691
- Company Name: Lundell Manufacturing Corp
- Inspection Date: 2016-11-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/lundell-manufacturing-corp/12d73bdf-694a-4929-9ff7-51be7d8dd0f0

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