# FDA Inspection 597702 - Technolas Perfect Vision GmbH - July 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/technolas-perfect-vision-gmbh/aa023161-b3f8-470e-92c4-e106e201e7fa
Source feed: FDA_Inspections

> FDA Inspection 597702 for Technolas Perfect Vision GmbH on July 23, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 597702
- Company Name: Technolas Perfect Vision GmbH
- Inspection Date: 2009-07-23
- 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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- [FDA Inspection 702560 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/technolas-perfect-vision-gmbh/0b937dc9-b076-4e9c-a857-6034601a078d)
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- [FDA Inspection 597702 - 2009-07-23](https://www.keypedia.com/records/fda_inspections/technolas-perfect-vision-gmbh/5e977b31-6c00-4771-8bdd-2c208aa118fa)

Company: https://www.keypedia.com/companies/technolas-perfect-vision-gmbh/4429d910-1dfa-4f0d-98f0-c9dc90d3d37d

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