Natureplex, LLC
FDA inspection history across 2 sites, 2004 to 2025
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2004: one warning letter; 2019: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2004One warning letter, at Memphis, Tennessee.
- 2019One Form 483, at Olive Branch, Mississippi.
- 2025One Form 483, at Olive Branch, Mississippi.
- 2025The longest 483 on file: 2 observations over 39 pages at Olive Branch, Mississippi.
Cited most
Across all Natureplex observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.194(a)(4)Laboratory records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Natureplex file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Olive Branch, Mississippi
Two Form 483s · 2019 to 2025 · 4 observations
Latest: Form 483, Jul 24, 2025 →Memphis, Tennessee
One warning letter · 2004
Latest: Warning letter, Aug 18, 2004 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-24 | 483 Form 483 | Olive Branch, Mississippi | 2 | $99 |
| 2019-12-20 | 483 Form 483 | Olive Branch, Mississippi | 2 | $99 |
| 2004-08-18 | Warning letter Warning letter | Memphis, Tennessee | — | $99 |
Investigators on these documents
Brittny C. Cargo (1)Steven J. Rush (1)Tracy J. Washington (1)
FEI number 3003631744 · most recent document Jul 24, 2025
About Natureplex, LLC
How many FDA Form 483s has Natureplex, LLC received?
FDA Intel has 2 Form 483s on file for Natureplex, LLC; the most recent is dated Jul 24, 2025.
When was Natureplex, LLC last inspected by FDA?
The most recent FDA inspection document on file for Natureplex, LLC is a Form 483 dated Jul 24, 2025, for the site in Olive Branch, Mississippi.
What did FDA cite at Natureplex, LLC?
The regulations cited most in the observations on file for Natureplex, LLC are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.194(a)(4) (Laboratory records), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.
Has Natureplex, LLC received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Natureplex, LLC; the most recent is dated Aug 18, 2004.