# FDA Inspection 732112 - Bioteque America, Inc. - June 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/bioteque-america-inc/b90b395f-9ec7-4f0b-912c-845a92677b0f
Source feed: FDA_Inspections

> FDA Inspection 732112 for Bioteque America, Inc. on June 24, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 732112
- Company Name: Bioteque America, Inc.
- Inspection Date: 2011-06-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 840273 - 2013-07-15](https://www.keypedia.com/records/fda_inspections/bioteque-america-inc/a768cb96-a8da-4a93-943e-62559d310ed4)
- [FDA Inspection 732112 - 2011-06-24](https://www.keypedia.com/records/fda_inspections/bioteque-america-inc/ee5f21b0-c37e-4cfb-b6a7-f50e185b4303)

Company: https://www.keypedia.com/companies/bioteque-america-inc/886f7066-b209-4519-b7d7-430006aa13b3

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