# BioElectronics Corporation, Frederick, MD – FDA Inspections

Source: https://www.keypedia.com/companies/bioelectronics-corporation/ebbf1432-07a9-484e-b8d6-a1051bbf15ca

> Inspection records and compliance data for BioElectronics Corporation in Frederick, Maryland. 4 FDA inspections on record, 1 Form 483, 1 warning letter, last inspected July 10, 2026.

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## Details

- Name: BioElectronics Corporation
- FEI Number: 3005550216
- Address Line 1: 4539 Metropolitan Ct
- City: Frederick
- State: Maryland
- Zip Code: 21704
- Country Name: United States
- Address: 4539 Metropolitan Ct, Frederick, Maryland 21704, United States
- Country: United States

## Related Documents

- FDA Inspection 1328376 - BioElectronics Corporation - 2026-07-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2026
- [FDA Inspection 1328376 - BioElectronics Corporation - 2026-07-10](https://www.keypedia.com/records/fda_inspections/bioelectronics-corporation/39fe88b0-e07c-48a2-bd64-586a2a86ca62) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2026
- FDA Inspection 1123763 - BioElectronics Corporation - 2020-01-16 — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2020
- [FDA Inspection 934351 - BioElectronics Corporation - 2015-07-14](https://www.keypedia.com/records/fda_inspections/bioelectronics-corporation/57bf0686-3893-4f62-a290-a932c78029b5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2015
- FDA Inspection 934351 - BioElectronics Corporation - 2015-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2015
- [WARNING_LETTER - BioElectronics Corporation - 2012-01-31](https://www.keypedia.com/records/warning_letter/bioelectronics-corporation/6f105c7c-f021-46cb-9d5f-c233d248da0a) — source: FDA, date: January 31, 2012
- [FDA Inspection 576907 - BioElectronics Corporation - 2009-04-28](https://www.keypedia.com/records/fda_inspections/bioelectronics-corporation/e74c1f2b-7ba1-4416-8099-cd16b0a077df) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2009

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