# Acuderm, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/acuderm-inc/9dd97a4d-a9f0-4ae2-8c49-d9b4765fe034

> Inspection records and compliance data for Acuderm, Inc. in Ft Lauderdale, Florida. Access full analysis and detailed observations.

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## Details

- Name: Acuderm, Inc.
- FEI Number: 1035236
- City: Ft Lauderdale
- State: Florida
- Country Name: United States
- Address Line 1: 6555 Powerline Rd
- Zip Code: 33309

## Related Documents

- [FDA Inspection 1017933 - Acuderm, Inc. - 2017-07-13](https://www.keypedia.com/records/fda_inspections/acuderm-inc/b8ae7ad1-3de0-4869-91dd-36d573b6b2fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 13, 2017
- [FDA Inspection 1017933 - Acuderm, Inc. - 2017-07-13](https://www.keypedia.com/records/fda_inspections/acuderm-inc/97e26a06-4f30-4b31-bf40-4effa4018f92) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 13, 2017
- [FDA Inspection 878759 - Acuderm, Inc. - 2014-05-09](https://www.keypedia.com/records/fda_inspections/acuderm-inc/9cd6b73e-b7ea-429a-a3c7-03c82ebd8c26) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2014
- [FDA Inspection 878759 - Acuderm, Inc. - 2014-05-09](https://www.keypedia.com/records/fda_inspections/acuderm-inc/fc45bf3e-8f2e-4760-89f4-6e6307c32c6f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2014
- [FDA Inspection 646620 - Acuderm, Inc. - 2010-02-19](https://www.keypedia.com/records/fda_inspections/acuderm-inc/d956a69c-b20d-4c68-90ae-45bb2e9ed9d2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2010
- [FDA Inspection 646620 - Acuderm, Inc. - 2010-02-19](https://www.keypedia.com/records/fda_inspections/acuderm-inc/bede169d-b8b1-4955-a9a0-04924ed8c15a) — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2010
- [FDA Inspection 646620 - Acuderm, Inc. - 2010-02-19](https://www.keypedia.com/records/fda_inspections/acuderm-inc/4554c574-a044-431a-93f5-049385583bf4) — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2010

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