# FDA Inspection 845219 - Boehringer Laboratories, Inc. - August 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/boehringer-laboratories-inc/7d204b79-64fd-4de6-b9eb-4e9486ee55d6
Source feed: FDA_Inspections

> FDA Inspection 845219 for Boehringer Laboratories, Inc. on August 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 845219
- Company Name: Boehringer Laboratories, Inc.
- Inspection Date: 2013-08-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 845219 - 2013-08-13](https://www.keypedia.com/records/fda_inspections/boehringer-laboratories-inc/581703c3-9c61-48a3-9f4d-d4094fdc41d3)
- [FDA Inspection 751939 - 2011-11-07](https://www.keypedia.com/records/fda_inspections/boehringer-laboratories-inc/c036322e-8f3c-4f84-bf86-990a3875bb6f)
- [FDA Inspection 751939 - 2011-11-07](https://www.keypedia.com/records/fda_inspections/boehringer-laboratories-inc/8652ca16-81db-4ad0-b0bd-99e75c339058)

Company: https://www.keypedia.com/companies/boehringer-laboratories-inc/7c3da463-ea98-4e9a-92cf-31a702872932

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