# DUSA Pharmaceuticals, Inc. – FDA Inspection, Sep 8, 2023

Source: https://www.keypedia.com/records/fda_inspections/dusa-pharmaceuticals-inc/473e61bf-5426-48c4-a8a0-9785e8266127
Source feed: FDA_Inspections

> FDA inspection 1217179 of DUSA Pharmaceuticals, Inc., September 08, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1217179
- Company Name: DUSA Pharmaceuticals, Inc.
- Inspection Date: 2023-09-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 986674 - 2016-09-22
- FDA Inspection 934706 - 2015-05-29
- [FDA Inspection 788414 - 2012-06-20](https://www.keypedia.com/records/fda_inspections/dusa-pharmaceuticals-inc/7c7cb1ec-2fb2-43a7-af20-0e7060e3d401)
- FDA Inspection 777605 - 2012-04-18
- [FDA Inspection 649444 - 2010-03-04](https://www.keypedia.com/records/fda_inspections/dusa-pharmaceuticals-inc/86179c65-85f8-4949-bdd8-212d4c125fa5)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

Company: https://www.keypedia.com/companies/dusa-pharmaceuticals-inc/477fe89d-b607-4aae-82b5-23a02cca9bd0

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