FDA Inspection
LNK International, Inc.LNK International, Inc. – FDA Inspection, Jan 26, 2011
Record Details
This FDA Inspection record concerns LNK International, Inc., with an inspection on January 26, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- LNK International, Inc.
- Inspection Date
- January 26, 2011
- Product Type
- Drugs
View Company Profile
ID · 7758169b-b3a6-4363-8416-ce009639609e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 713044
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
- 21 CFR 606.100(c)Thorough investigations
- 21 CFR 211.22(a)Authority lacking to review records, investigate errors
- 21 CFR 211.100(b)SOPs not followed / documented
Full citation text and observation details available on the Dashboard.
Other FDA inspections of LNK International, Inc.
16| Date | Classification | Office | Project area |
|---|---|---|---|
| August 27, 2026 | Not classified | New York District Office | |
| October 28, 2025 | VAI | New York District Office | Drug Quality Assurance |
| July 1, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 8, 2019 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 7, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for LNK International, Inc.
- FDA Inspection 1288018 - 2026-08-27
- FDA Inspection 1281600 - 2025-10-28
- FDA Inspection 1145956 - 2021-07-01
- FDA Inspection 1078694 - 2019-02-08
- FDA Inspection 1007918 - 2017-03-07
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