# Keyser Brothers Incorporated - Inspection Records

Source: https://www.keypedia.com/companies/keyser-brothers-incorporated/d5c02267-2a1e-4d47-abb8-852bf125da35

> Inspection records and compliance data for Keyser Brothers Incorporated in Lottsburg, Virginia. Access full analysis and detailed observations.

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## Details

- Name: Keyser Brothers Incorporated
- FEI Number: 1110882
- City: Lottsburg
- State: Virginia
- Country Name: United States
- Address Line 1: 965 Honest Point Rd
- Zip Code: 22511

## Related Documents

- [FDA Inspection 874293 - Keyser Brothers Incorporated - 2014-04-02](https://www.keypedia.com/records/fda_inspections/keyser-brothers-incorporated/9010a238-6fbb-4d24-9824-a13d64131aa3) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2014
- [WARNING_LETTER - Keyser Brothers Incorporated - 2013-08-13](https://www.keypedia.com/records/warning_letter/keyser-brothers-incorporated/57399d22-1d8a-43ad-af28-b9e176e25d7e) — source: FDA, date: August 13, 2013
- [FDA Inspection 843576 - Keyser Brothers Incorporated - 2013-08-13](https://www.keypedia.com/records/fda_inspections/keyser-brothers-incorporated/98306926-a878-4ec0-af38-6108eb844329) — classification: Official Action Indicated (OAI), source: FDA, date: August 13, 2013
- [FDA Inspection 675664 - Keyser Brothers Incorporated - 2010-08-11](https://www.keypedia.com/records/fda_inspections/keyser-brothers-incorporated/a3488cfc-c85c-4acf-b115-a88b7d76b21c) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2010
- [FDA Inspection 675664 - Keyser Brothers Incorporated - 2010-08-11](https://www.keypedia.com/records/fda_inspections/keyser-brothers-incorporated/80a08648-0f26-4d09-8d30-ed2401c104a5) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2010
- [FDA Inspection 614023 - Keyser Brothers Incorporated - 2009-09-24](https://www.keypedia.com/records/fda_inspections/keyser-brothers-incorporated/0afd9bfa-d97f-410f-9bbd-171965d62785) — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2009

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