# LKC Technologies, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/lkc-technologies-inc/5721e30b-8087-4450-8f88-bec14f6d71c9

> Inspection records and compliance data for LKC Technologies, Inc. in Gaithersburg, Maryland. Access full analysis and detailed observations.

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## Details

- Name: LKC Technologies, Inc.
- FEI Number: 1119189
- City: Gaithersburg
- State: Maryland
- Country Name: United States
- Address Line 1: 2 Professional Dr Ste 222
- Zip Code: 20879

## Related Documents

- [FDA Inspection 1046213 - LKC Technologies, Inc. - 2018-03-29](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/8fe26ffe-5e01-4be2-94f7-52d01fc9781f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 29, 2018
- [FDA Inspection 1046213 - LKC Technologies, Inc. - 2018-03-29](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/51098a7b-ad03-4620-9785-968bba9bdbec) — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2018
- [FDA Inspection 860090 - LKC Technologies, Inc. - 2013-12-17](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/eb098070-50e2-43dd-ae9c-fc9529705c1d) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- [FDA Inspection 860090 - LKC Technologies, Inc. - 2013-12-17](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/f9566e3e-a3a1-47bb-a7de-71771b53930a) — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- [FDA Inspection 646653 - LKC Technologies, Inc. - 2010-03-05](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/2e4960b9-9293-429a-a3c2-766c1306f919) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2010
- [FDA Inspection 646653 - LKC Technologies, Inc. - 2010-03-05](https://www.globalkeysolutions.net/records/fda_inspections/lkc-technologies-inc/1187f7e5-4d9e-4d34-86d7-bf07878d1495) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2010

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