Greer Laboratories, Inc.
FDA inspection history in Lenoir, North Carolina, 2013 to 2024
- 5
- Form 483s
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2013: one Form 483; 2014: one warning letter; 2015: one Form 483; 2019: one Form 483; 2022: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2013–15Two Form 483s and one warning letter, at Lenoir, North Carolina.
- 2015The longest 483 on file: 11 observations over 9 pages at Lenoir, North Carolina.
- 2019One Form 483, at Lenoir, North Carolina.
- 2022–24Two Form 483s, at Lenoir, North Carolina.
Cited most
Across all Greer Laboratories observations on file
- 21 CFR 211.42Design and construction features5
- 21 CFR 211.113Control of microbiological contamination4
- 21 CFR 211.160General requirements3
- 21 CFR 211.192Production record review3
- 21 CFR 211.100Written procedures; deviations2
The complete Greer Laboratories file.
All 6 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
Lenoir, North Carolina
Five Form 483s and one warning letter · 2013 to 2024 · 37 observations
Latest: Form 483, Dec 18, 2024 →
Documents
6 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-18 | 483 Form 483 | Lenoir, North Carolina | 5 | $99 |
| 2022-11-01 | 483 Form 483 | Lenoir, North Carolina | 7 | $99 |
| 2019-09-11 | 483 Form 483 | Lenoir, North Carolina | 4 | $99 |
| 2015-08-27 | 483 Form 483 | Lenoir, North Carolina | 11 | $99 |
| 2014-04-21 | Warning letter Warning letter | Lenoir, North Carolina | — | $99 |
| 2013-01-15 | 483 Form 483 | Lenoir, North Carolina | 10 | $99 |
Investigators on these documents
FEI number 1011574 · most recent document Dec 18, 2024
About Greer Laboratories, Inc.
How many FDA Form 483s has Greer Laboratories, Inc. received?
FDA Intel has 5 Form 483s on file for Greer Laboratories, Inc.; the most recent is dated Dec 18, 2024.
When was Greer Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Greer Laboratories, Inc. is a Form 483 dated Dec 18, 2024, for the site in Lenoir, North Carolina.
What did FDA cite at Greer Laboratories, Inc.?
The regulations cited most in the observations on file for Greer Laboratories, Inc. are 21 CFR 211.42 (Design and construction features), 5 times; 21 CFR 211.113 (Control of microbiological contamination), 4 times; 21 CFR 211.160 (General requirements), 3 times.
Has Greer Laboratories, Inc. received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Greer Laboratories, Inc.; the most recent is dated Apr 21, 2014.