# FDA Inspection 780592 - Kontur Kontact Lens Co., Inc. - May 08, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/kontur-kontact-lens-co-inc/df9b84d9-0b8b-4239-849e-cdfa84908da0
Source feed: FDA_Inspections

> FDA Inspection 780592 for Kontur Kontact Lens Co., Inc. on May 08, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 780592
- Company Name: Kontur Kontact Lens Co., Inc.
- Inspection Date: 2012-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/kontur-kontact-lens-co-inc/de6a4706-b35d-43fc-9c4c-334bef1ba16a

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