# FDA Inspection 671018 - Penniman & Browne, Inc. - July 09, 2010

Source: https://www.keypedia.com/records/fda_inspections/penniman-browne-inc/0c5dff28-9607-44e8-9e75-fa211a871237
Source feed: FDA_Inspections

> FDA Inspection 671018 for Penniman & Browne, Inc. on July 09, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 671018
- Company Name: Penniman & Browne, Inc.
- Inspection Date: 2010-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 671018 - 2010-07-09](https://www.keypedia.com/records/fda_inspections/penniman-browne-inc/f515b0d3-cf62-45dd-a37c-9df9cd4106a3)

Company: https://www.keypedia.com/companies/penniman-browne-inc/75133e0a-c8eb-4da9-b02c-126f480990dc

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